9-23730999-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23730999
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23730999
    reference: chr 9
allele count: 2
allele frequency: 2.050398802567099e-5
allele num: 97542
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.333+21T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.333+21T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.333+21T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.333+21T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.420+21T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.333+21T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-73+21T>C
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4822
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11364
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32973
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1195
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3214
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2400
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 631
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/9-23731008-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731008
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731008
    reference: chr 9
allele count: 1
allele frequency: 9.278675747397332e-6
allele num: 107774
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.333+12G>T
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.333+12G>T
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.333+12G>T
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.333+12G>T
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.420+12G>T
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.333+12G>T
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-73+12G>T
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40369
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6489
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5995
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 931
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 679
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum

9-23731010-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731010
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731010
    reference: chr 9
allele count: 1
allele frequency: 9.121923631255359e-6
allele num: 109626
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.333+10A>T
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.420+10A>T
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.333+10A>T
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.333+10A>T
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-73+10A>T
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.333+10A>T
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.333+10A>T
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5640
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41584
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6147
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 779
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 696
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3217
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43362
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 835
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

9-23731010-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731010
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731010
    reference: chr 9
allele count: 1
allele frequency: 9.121923631255359e-6
allele num: 109626
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.333+10A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.333+10A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.420+10A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.333+10A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-73+10A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.333+10A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.333+10A>G
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6147
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5640
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41584
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5564
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 835
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43362
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

9-23731025-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731025
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731025
    reference: chr 9
allele count: 2
allele frequency: 1.69548999660902e-5
allele num: 117960
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.328A>G
  hgvsp: ENSP00000380479.2:p.Ile110Val
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.328A>G
  hgvsp: ENSP00000440998.1:p.Ile110Val
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-78A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.328A>G
  hgvsp: ENSP00000412602.1:p.Ile110Val
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.415A>G
  hgvsp: ENSP00000369453.4:p.Ile139Val
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.328A>G
  hgvsp: ENSP00000223951.5:p.Ile110Val
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.328A>G
  hgvsp: ENSP00000369460.1:p.Ile110Val
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7488
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 746
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49170
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ile110Val
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP

9-23731032-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731032
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731032
    reference: chr 9
allele count: 1
allele frequency: 8.373245805003851e-6
allele num: 119428
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.408C>G
  hgvsp: ENST00000380110.4:c.408C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-85C>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.321C>G
  hgvsp: ENST00000544538.1:c.321C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.321C>G
  hgvsp: ENST00000223951.6:c.321C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.321C>G
  hgvsp: ENST00000380117.1:c.321C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.321C>G
  hgvsp: ENST00000440102.1:c.321C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.321C>G
  hgvsp: ENST00000397312.2:c.321C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46585
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7782
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50346
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3217
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr107Thr
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP

9-23731056-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731056
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731056
    reference: chr 9
allele count: 1
allele frequency: 8.299581701082266e-6
allele num: 120488
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.384C>G
  hgvsp: ENST00000380110.4:c.384C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.297C>G
  hgvsp: ENST00000380117.1:c.297C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.297C>G
  hgvsp: ENST00000544538.1:c.297C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.297C>G
  hgvsp: ENST00000440102.1:c.297C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-109C>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.297C>G
  hgvsp: ENST00000397312.2:c.297C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.297C>G
  hgvsp: ENST00000223951.6:c.297C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8280
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3402
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3220
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Thr99Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff

9-23731059-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731059
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731059
    reference: chr 9
allele count: 1
allele frequency: 8.296414289743973e-6
allele num: 120534
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.381C>T
  hgvsp: ENST00000380110.4:c.381C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.294C>T
  hgvsp: ENST00000397312.2:c.294C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.294C>T
  hgvsp: ENST00000440102.1:c.294C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.294C>T
  hgvsp: ENST00000223951.6:c.294C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.294C>T
  hgvsp: ENST00000380117.1:c.294C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-112C>T
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.294C>T
  hgvsp: ENST00000544538.1:c.294C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46694
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3220
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3403
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 768
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51035
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asn98Asn
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

9-23731064-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731064
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731064
    reference: chr 9
allele count: 3
allele frequency: 2.487892257679294e-5
allele num: 120584
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.289A>G
  hgvsp: ENSP00000223951.5:p.Ile97Val
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.289A>G
  hgvsp: ENSP00000380479.2:p.Ile97Val
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.289A>G
  hgvsp: ENSP00000369460.1:p.Ile97Val
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.376A>G
  hgvsp: ENSP00000369453.4:p.Ile126Val
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.289A>G
  hgvsp: ENSP00000412602.1:p.Ile97Val
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.289A>G
  hgvsp: ENSP00000440998.1:p.Ile97Val
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-117A>G
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46698
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3222
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ile97Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

9-23731068-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731068
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731068
    reference: chr 9
allele count: 3
allele frequency: 2.486737400530504e-5
allele num: 120640
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-121A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.285A>G
  hgvsp: ENST00000440102.1:c.285A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.285A>G
  hgvsp: ENST00000544538.1:c.285A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.285A>G
  hgvsp: ENST00000397312.2:c.285A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.372A>G
  hgvsp: ENST00000380110.4:c.372A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.285A>G
  hgvsp: ENST00000223951.6:c.285A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.285A>G
  hgvsp: ENST00000380117.1:c.285A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8373
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 769
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Lys95Lys
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff

9-23731071-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731071
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731071
    reference: chr 9
allele count: 2
allele frequency: 1.657769967839263e-5
allele num: 120644
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-124G>A
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.282G>A
  hgvsp: ENST00000544538.1:c.282G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.369G>A
  hgvsp: ENST00000380110.4:c.369G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.282G>A
  hgvsp: ENST00000397312.2:c.282G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.282G>A
  hgvsp: ENST00000223951.6:c.282G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.282G>A
  hgvsp: ENST00000440102.1:c.282G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.282G>A
  hgvsp: ENST00000380117.1:c.282G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8387
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46665
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 769
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu94Glu
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

9-23731072-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731072
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731072
    reference: chr 9
allele count: 1
allele frequency: 8.289124668435012e-6
allele num: 120640
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.281A>G
  hgvsp: ENSP00000412602.1:p.Glu94Gly
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.368A>G
  hgvsp: ENSP00000369453.4:p.Glu123Gly
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-125A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.281A>G
  hgvsp: ENSP00000369460.1:p.Glu94Gly
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.281A>G
  hgvsp: ENSP00000440998.1:p.Glu94Gly
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.281A>G
  hgvsp: ENSP00000380479.2:p.Glu94Gly
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.281A>G
  hgvsp: ENSP00000223951.5:p.Glu94Gly
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46665
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 784
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3417
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3219
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu94Gly
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

9-23731073-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731073
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731073
    reference: chr 9
allele count: 5
allele frequency: 4.144424919598156e-5
allele num: 120644
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.280G>A
  hgvsp: ENSP00000412602.1:p.Glu94Lys
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.280G>A
  hgvsp: ENSP00000440998.1:p.Glu94Lys
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.280G>A
  hgvsp: ENSP00000380479.2:p.Glu94Lys
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.280G>A
  hgvsp: ENSP00000369460.1:p.Glu94Lys
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.367G>A
  hgvsp: ENSP00000369453.4:p.Glu123Lys
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-126G>A
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.280G>A
  hgvsp: ENSP00000223951.5:p.Glu94Lys
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8387
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46657
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu94Lys
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

9-23731077-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731077
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731077
    reference: chr 9
allele count: 1
allele frequency: 8.288300235387727e-6
allele num: 120652
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.276T>A
  hgvsp: ENSP00000440998.1:p.Asp92Glu
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.276T>A
  hgvsp: ENSP00000380479.2:p.Asp92Glu
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.276T>A
  hgvsp: ENSP00000369460.1:p.Asp92Glu
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.363T>A
  hgvsp: ENSP00000369453.4:p.Asp121Glu
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.276T>A
  hgvsp: ENSP00000412602.1:p.Asp92Glu
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.276T>A
  hgvsp: ENSP00000223951.5:p.Asp92Glu
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-130T>A
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46611
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1730
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8444
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp92Glu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

9-23731083-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731083
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731083
    reference: chr 9
allele count: 2
allele frequency: 1.658017342861406e-5
allele num: 120626
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.270C>A
  hgvsp: ENST00000380117.1:c.270C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.357C>A
  hgvsp: ENST00000380110.4:c.357C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.270C>A
  hgvsp: ENST00000544538.1:c.270C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.270C>A
  hgvsp: ENST00000223951.6:c.270C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.270C>A
  hgvsp: ENST00000397312.2:c.270C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.270C>A
  hgvsp: ENST00000440102.1:c.270C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-136C>A
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46500
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8476
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 771
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3217
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 50988
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro90Pro
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

9-23731084-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731084
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731084
    reference: chr 9
allele count: 1
allele frequency: 8.290911502810618e-6
allele num: 120614
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.269C>A
  hgvsp: ENSP00000223951.5:p.Pro90His
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.269C>A
  hgvsp: ENSP00000380479.2:p.Pro90His
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.269C>A
  hgvsp: ENSP00000440998.1:p.Pro90His
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.356C>A
  hgvsp: ENSP00000369453.4:p.Pro119His
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-137C>A
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.269C>A
  hgvsp: ENSP00000369460.1:p.Pro90His
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.269C>A
  hgvsp: ENSP00000412602.1:p.Pro90His
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46457
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8497
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3421
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro90His
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

9-23731090-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731090
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731090
    reference: chr 9
allele count: 1
allele frequency: 8.2917364554485e-6
allele num: 120602
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.350T>A
  hgvsp: ENSP00000369453.4:p.Ile117Asn
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-143T>A
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.263T>A
  hgvsp: ENSP00000440998.1:p.Ile88Asn
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.263T>A
  hgvsp: ENSP00000380479.2:p.Ile88Asn
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.263T>A
  hgvsp: ENSP00000223951.5:p.Ile88Asn
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.263T>A
  hgvsp: ENSP00000369460.1:p.Ile88Asn
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.263T>A
  hgvsp: ENSP00000412602.1:p.Ile88Asn
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 768
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50930
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ile88Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP

9-23731092-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731092
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731092
    reference: chr 9
allele count: 1
allele frequency: 8.29242404139578e-6
allele num: 120592
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.348C>T
  hgvsp: ENST00000380110.4:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-145C>T
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.261C>T
  hgvsp: ENST00000544538.1:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.261C>T
  hgvsp: ENST00000440102.1:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.261C>T
  hgvsp: ENST00000223951.6:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.261C>T
  hgvsp: ENST00000397312.2:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.261C>T
  hgvsp: ENST00000380117.1:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46296
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1750
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8551
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3418
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50870
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Tyr87Tyr
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD

9-23731095-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731095
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731095
    reference: chr 9
allele count: 1
allele frequency: 8.295726041943191e-6
allele num: 120544
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.258C>T
  hgvsp: ENST00000544538.1:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.345C>T
  hgvsp: ENST00000380110.4:c.345C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-148C>T
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.258C>T
  hgvsp: ENST00000380117.1:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.258C>T
  hgvsp: ENST00000223951.6:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.258C>T
  hgvsp: ENST00000440102.1:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.258C>T
  hgvsp: ENST00000397312.2:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46194
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8560
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3414
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn86Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

9-23731122-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731122
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731122
    reference: chr 9
allele count: 1
allele frequency: 8.381246123673667e-6
allele num: 119314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.231G>A
  hgvsp: ENST00000380117.1:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.318G>A
  hgvsp: ENST00000380110.4:c.318G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-175G>A
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.231G>A
  hgvsp: ENST00000440102.1:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.231G>A
  hgvsp: ENST00000223951.6:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.231G>A
  hgvsp: ENST00000544538.1:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.231G>A
  hgvsp: ENST00000397312.2:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3312
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 732
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48235
  bin: 6.25e1
  variant carriers: 0
hgvs: c.231G>A
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

9-23731128-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731128
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731128
    reference: chr 9
allele count: 1
allele frequency: 8.428860418071477e-6
allele num: 118640
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.230-5A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.230-5A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.230-5A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.317-5A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.230-5A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-176-5A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.230-5A>G
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41737
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 708
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3216
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 700
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
hgvs: c.230-5A>G
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum

9-23731142-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731142
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731142
    reference: chr 9
allele count: 3
allele frequency: 2.595245510225267e-5
allele num: 115596
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.230-19T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.317-19T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-176-19T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.230-19T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.230-19T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.230-19T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.230-19T>C
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2375
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3479
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8015
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31876
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3218
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 6973
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3151
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2480
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/9-23731144-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731144
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731144
    reference: chr 9
allele count: 1
allele frequency: 8.641548565502938e-6
allele num: 115720
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-176-21T>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.317-21T>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.230-21T>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.230-21T>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.230-21T>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.230-21T>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.230-21T>G
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7907
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10369
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30608
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4027
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2142
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34005
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7543
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2507
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 587
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum

9-23731146-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731146
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731146
    reference: chr 9
allele count: 1
allele frequency: 8.665661449938475e-6
allele num: 115398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.230-23T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.317-23T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.230-23T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.230-23T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.230-23T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-176-23T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.230-23T>C
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2572
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4460
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10929
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29586
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7762
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33115
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7793
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3967
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ

9-23731147-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731147
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731147
    reference: chr 9
allele count: 1
allele frequency: 8.676337891302839e-6
allele num: 115256
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.230-24C>T
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.317-24C>T
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.230-24C>T
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.230-24C>T
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.230-24C>T
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-176-24C>T
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.230-24C>T
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4927
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28645
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11548
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4257
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2583
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3020
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3215
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 768
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

9-23731150-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731150
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731150
    reference: chr 9
allele count: 1
allele frequency: 8.703068702024334e-6
allele num: 114902
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.317-27T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.230-27T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.230-27T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-176-27T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.230-27T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.230-27T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.230-27T>C
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6536
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2772
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25710
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1006
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3367
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 833
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3215
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8667
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 611
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

9-23731152-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731152
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731152
    reference: chr 9
allele count: 1
allele frequency: 8.720676724513823e-6
allele num: 114670
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.230-29T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.230-29T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.230-29T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-176-29T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.230-29T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.317-29T>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.230-29T>C
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14051
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7965
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6834
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1239
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5879
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3993
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8937
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3215
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3811
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

9-23731153-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731153
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731153
    reference: chr 9
allele count: 2
allele frequency: 1.752019202130455e-5
allele num: 114154
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.230-30A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.230-30A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.317-30A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.230-30A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.230-30A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.230-30A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-176-30A>G
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6298
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10214
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21049
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14896
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1005
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1489
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4116
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6694
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: T
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

9-23731153-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731153
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731153
    reference: chr 9
allele count: 28
allele frequency: 2.452826882982637e-4
allele num: 114154
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.230-30A>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.230-30A>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.230-30A>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.230-30A>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-176-30A>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.230-30A>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.317-30A>C
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21049
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10214
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6298
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14896
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6694
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1489
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9085
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1005
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3239
  bin: 9.75e1
  variant carriers: 24
genotype quality: GenotypeQuality
  all individuals: 4116
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1993
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 1
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

9-23731158-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731158
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731158
    reference: chr 9
allele count: 9
allele frequency: 7.973916433355778e-5
allele num: 112868
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.230-35C>A
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.230-35C>A
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.317-35C>A
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-176-35C>A
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.230-35C>A
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.230-35C>A
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.230-35C>A
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15349
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16322
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3357
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15177
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5251
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8970
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1547
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1629
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15583
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4464
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

9-23731160-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731160
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731160
    reference: chr 9
allele count: 11
allele frequency: 9.738477610354657e-5
allele num: 112954
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.230-37A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.230-37A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.230-37A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.230-37A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-176-37A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.317-37A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.230-37A>G
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5223
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15365
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16454
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 15113
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9134
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 593
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 612
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2758
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7793
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6829
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3225
  bin: 9.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 1272
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

16-69875981-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69875981
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69875981
    reference: chr 16
allele count: 32
allele frequency: 2.93357290845419e-4
allele num: 109082
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000348283
  ensembl transcript: ENST00000356003
  gene symbol: WWP2
  hgvsc: ENST00000356003.2:c.533G>A
  hgvsp: ENSP00000348283.2:p.Arg178Gln
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000352069
  ensembl transcript: ENST00000359154
  gene symbol: WWP2
  hgvsc: ENST00000359154.2:c.533G>A
  hgvsp: ENSP00000352069.2:p.Arg178Gln
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000563618
  gene symbol: WWP2
  hgvsc: ENST00000563618.1:n.346G>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000455311
  ensembl transcript: ENST00000569174
  gene symbol: WWP2
  hgvsc: ENST00000569174.1:c.533G>A
  hgvsp: ENSP00000455311.1:p.Arg178Gln
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000396871
  ensembl transcript: ENST00000448661
  gene symbol: WWP2
  hgvsc: ENST00000448661.1:c.533G>A
  hgvsp: ENSP00000396871.1:p.Arg178Gln
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000445616
  ensembl transcript: ENST00000542271
  gene symbol: WWP2
  hgvsc: ENST00000542271.1:c.185G>A
  hgvsp: ENSP00000445616.1:p.Arg62Gln
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000567986
  gene symbol: WWP2
  hgvsc: ENST00000567986.1:n.443G>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000544162
  gene symbol: WWP2
  hgvsc: ENST00000544162.1:n.405G>A
  variant of: http://identifiers.org/hgnc/16804
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5693
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2512
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10302
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 703
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1141
  bin: 9.75e1
  variant carriers: 32
genotype quality: GenotypeQuality
  all individuals: 557
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg178Gln
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

16-69875985-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69875985
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69875985
    reference: chr 16
allele count: 1
allele frequency: 9.226624347216328e-6
allele num: 108382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000396871
  ensembl transcript: ENST00000448661
  gene symbol: WWP2
  hgvsc: ENST00000448661.1:c.537C>T
  hgvsp: ENST00000448661.1:c.537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000544162
  gene symbol: WWP2
  hgvsc: ENST00000544162.1:n.409C>T
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000567986
  gene symbol: WWP2
  hgvsc: ENST00000567986.1:n.447C>T
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000455311
  ensembl transcript: ENST00000569174
  gene symbol: WWP2
  hgvsc: ENST00000569174.1:c.537C>T
  hgvsp: ENST00000569174.1:c.537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000445616
  ensembl transcript: ENST00000542271
  gene symbol: WWP2
  hgvsc: ENST00000542271.1:c.189C>T
  hgvsp: ENST00000542271.1:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000348283
  ensembl transcript: ENST00000356003
  gene symbol: WWP2
  hgvsc: ENST00000356003.2:c.537C>T
  hgvsp: ENST00000356003.2:c.537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000563618
  gene symbol: WWP2
  hgvsc: ENST00000563618.1:n.350C>T
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000352069
  ensembl transcript: ENST00000359154
  gene symbol: WWP2
  hgvsc: ENST00000359154.2:c.537C>T
  hgvsp: ENST00000359154.2:c.537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16804
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3054
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6042
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35315
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10454
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 954
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1193
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1111
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 39767
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 996
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
hgvs: p.His179His
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

16-69875991-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69875991
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69875991
    reference: chr 16
allele count: 488
allele frequency: 4.514923301815221e-3
allele num: 108086
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000455311
  ensembl transcript: ENST00000569174
  gene symbol: WWP2
  hgvsc: ENST00000569174.1:c.543C>T
  hgvsp: ENST00000569174.1:c.543C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000563618
  gene symbol: WWP2
  hgvsc: ENST00000563618.1:n.356C>T
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000348283
  ensembl transcript: ENST00000356003
  gene symbol: WWP2
  hgvsc: ENST00000356003.2:c.543C>T
  hgvsp: ENST00000356003.2:c.543C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000396871
  ensembl transcript: ENST00000448661
  gene symbol: WWP2
  hgvsc: ENST00000448661.1:c.543C>T
  hgvsp: ENST00000448661.1:c.543C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000445616
  ensembl transcript: ENST00000542271
  gene symbol: WWP2
  hgvsc: ENST00000542271.1:c.195C>T
  hgvsp: ENST00000542271.1:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000567986
  gene symbol: WWP2
  hgvsc: ENST00000567986.1:n.453C>T
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000544162
  gene symbol: WWP2
  hgvsc: ENST00000544162.1:n.415C>T
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000352069
  ensembl transcript: ENST00000359154
  gene symbol: WWP2
  hgvsc: ENST00000359154.2:c.543C>T
  hgvsp: ENST00000359154.2:c.543C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16804
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 1.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2306
  bin: 3.25e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 1.75e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 6139
  bin: 7.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 10685
  bin: 2.75e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 3.75e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 34496
  bin: 2.25e1
  variant carriers: 85
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 8.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 858
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 40257
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3165
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro181Pro
num of homozygotes: 3
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-69875994-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69875994
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69875994
    reference: chr 16
allele count: 5
allele frequency: 4.644164143337482e-5
allele num: 107662
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000352069
  ensembl transcript: ENST00000359154
  gene symbol: WWP2
  hgvsc: ENST00000359154.2:c.546C>T
  hgvsp: ENST00000359154.2:c.546C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000567986
  gene symbol: WWP2
  hgvsc: ENST00000567986.1:n.456C>T
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000563618
  gene symbol: WWP2
  hgvsc: ENST00000563618.1:n.359C>T
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000396871
  ensembl transcript: ENST00000448661
  gene symbol: WWP2
  hgvsc: ENST00000448661.1:c.546C>T
  hgvsp: ENST00000448661.1:c.546C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000455311
  ensembl transcript: ENST00000569174
  gene symbol: WWP2
  hgvsc: ENST00000569174.1:c.546C>T
  hgvsp: ENST00000569174.1:c.546C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000348283
  ensembl transcript: ENST00000356003
  gene symbol: WWP2
  hgvsc: ENST00000356003.2:c.546C>T
  hgvsp: ENST00000356003.2:c.546C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000445616
  ensembl transcript: ENST00000542271
  gene symbol: WWP2
  hgvsc: ENST00000542271.1:c.198C>T
  hgvsp: ENST00000542271.1:c.198C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000544162
  gene symbol: WWP2
  hgvsc: ENST00000544162.1:n.418C>T
  variant of: http://identifiers.org/hgnc/16804
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3643
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6341
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34125
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10766
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2313
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 820
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1107
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Pro182Pro
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum

16-69875996-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69875996
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69875996
    reference: chr 16
allele count: 2
allele frequency: 1.869438420698422e-5
allele num: 106984
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000563618
  gene symbol: WWP2
  hgvsc: ENST00000563618.1:n.361G>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000348283
  ensembl transcript: ENST00000356003
  gene symbol: WWP2
  hgvsc: ENST00000356003.2:c.548G>A
  hgvsp: ENSP00000348283.2:p.Ser183Asn
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000455311
  ensembl transcript: ENST00000569174
  gene symbol: WWP2
  hgvsc: ENST00000569174.1:c.548G>A
  hgvsp: ENSP00000455311.1:p.Ser183Asn
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000352069
  ensembl transcript: ENST00000359154
  gene symbol: WWP2
  hgvsc: ENST00000359154.2:c.548G>A
  hgvsp: ENSP00000352069.2:p.Ser183Asn
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000396871
  ensembl transcript: ENST00000448661
  gene symbol: WWP2
  hgvsc: ENST00000448661.1:c.548G>A
  hgvsp: ENSP00000396871.1:p.Ser183Asn
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000567986
  gene symbol: WWP2
  hgvsc: ENST00000567986.1:n.458G>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000445616
  ensembl transcript: ENST00000542271
  gene symbol: WWP2
  hgvsc: ENST00000542271.1:c.200G>A
  hgvsp: ENSP00000445616.1:p.Ser67Asn
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000544162
  gene symbol: WWP2
  hgvsc: ENST00000544162.1:n.420G>A
  variant of: http://identifiers.org/hgnc/16804
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33363
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10583
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4097
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6608
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39207
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 861
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 957
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 750
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9005
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser183Asn
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

16-69876001-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69876001
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69876001
    reference: chr 16
allele count: 1
allele frequency: 9.430403621274991e-6
allele num: 106040
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000455311
  ensembl transcript: ENST00000569174
  gene symbol: WWP2
  hgvsc: ENST00000569174.1:c.553A>G
  hgvsp: ENSP00000455311.1:p.Asn185Asp
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000445616
  ensembl transcript: ENST00000542271
  gene symbol: WWP2
  hgvsc: ENST00000542271.1:c.205A>G
  hgvsp: ENSP00000445616.1:p.Asn69Asp
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000348283
  ensembl transcript: ENST00000356003
  gene symbol: WWP2
  hgvsc: ENST00000356003.2:c.553A>G
  hgvsp: ENSP00000348283.2:p.Asn185Asp
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000567986
  gene symbol: WWP2
  hgvsc: ENST00000567986.1:n.463A>G
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000563618
  gene symbol: WWP2
  hgvsc: ENST00000563618.1:n.366A>G
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000396871
  ensembl transcript: ENST00000448661
  gene symbol: WWP2
  hgvsc: ENST00000448661.1:c.553A>G
  hgvsp: ENSP00000396871.1:p.Asn185Asp
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000352069
  ensembl transcript: ENST00000359154
  gene symbol: WWP2
  hgvsc: ENST00000359154.2:c.553A>G
  hgvsp: ENSP00000352069.2:p.Asn185Asp
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000544162
  gene symbol: WWP2
  hgvsc: ENST00000544162.1:n.425A>G
  variant of: http://identifiers.org/hgnc/16804
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32381
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7093
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10343
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1135
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3041
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 845
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asn185Asp
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

9-23731161-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731161
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731161
    reference: chr 9
allele count: 1
allele frequency: 8.884308534266778e-6
allele num: 112558
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.230-38G>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.230-38G>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.230-38G>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.317-38G>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-176-38G>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.230-38G>C
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.230-38G>C
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5249
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3452
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15107
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16381
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15368
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3215
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9178
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1621
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4439
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2754
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 656
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ
site quality: ClippingRankSum

9-23731162-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731162
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731162
    reference: chr 9
allele count: 241
allele frequency: 2.140167661267406e-3
allele num: 112608
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.317-39A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.230-39A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.230-39A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.230-39A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.230-39A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.230-39A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-176-39A>G
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15374
  bin: 1.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 9.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15753
  bin: 2.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 3.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 15954
  bin: 1.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 3.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3558
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4913
  bin: 2.75e1
  variant carriers: 34
genotype quality: GenotypeQuality
  all individuals: 16045
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3036
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3418
  bin: 9.75e1
  variant carriers: 231
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4488
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 3
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum

9-23731172-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23731172
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23731172
    reference: chr 9
allele count: 1
allele frequency: 9.177174531505241e-6
allele num: 108966
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.230-49T>A
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000391757
  ensembl transcript: ENST00000423281
  gene symbol: ELAVL2
  hgvsc: ENST00000423281.1:c.-176-49T>A
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.230-49T>A
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.317-49T>A
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.230-49T>A
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.230-49T>A
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.230-49T>A
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4849
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14702
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3612
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15428
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2225
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7997
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 763
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7220
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4565
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 772
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1426
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5741
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

9-23761956-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23761956
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 23761956
    reference: chr 9
allele count: 1
allele frequency: 9.320880636802566e-6
allele num: 107286
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000380479
  ensembl transcript: ENST00000397312
  gene symbol: ELAVL2
  hgvsc: ENST00000397312.2:c.229+48A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000412602
  ensembl transcript: ENST00000440102
  gene symbol: ELAVL2
  hgvsc: ENST00000440102.1:c.229+48A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369453
  ensembl transcript: ENST00000380110
  gene symbol: ELAVL2
  hgvsc: ENST00000380110.4:c.316+48A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000440998
  ensembl transcript: ENST00000544538
  gene symbol: ELAVL2
  hgvsc: ENST00000544538.1:c.229+48A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000369460
  ensembl transcript: ENST00000380117
  gene symbol: ELAVL2
  hgvsc: ENST00000380117.1:c.229+48A>G
  variant of: http://identifiers.org/hgnc/3313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107105
  ensembl protein: ENSP00000223951
  ensembl transcript: ENST00000223951
  gene symbol: ELAVL2
  hgvsc: ENST00000223951.6:c.229+48A>G
  variant of: http://identifiers.org/hgnc/3313
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14503
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3348
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10746
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5650
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7208
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4597
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10620
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1082
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 728
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4331
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4814
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6634
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4743
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2635
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2678
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1830
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 820
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-69876008-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69876008
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69876008
    reference: chr 16
allele count: 3
allele frequency: 2.885725278953444e-5
allele num: 103960
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000348283
  ensembl transcript: ENST00000356003
  gene symbol: WWP2
  hgvsc: ENST00000356003.2:c.560T>A
  hgvsp: ENSP00000348283.2:p.Phe187Tyr
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000567986
  gene symbol: WWP2
  hgvsc: ENST00000567986.1:n.470T>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000563618
  gene symbol: WWP2
  hgvsc: ENST00000563618.1:n.373T>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000445616
  ensembl transcript: ENST00000542271
  gene symbol: WWP2
  hgvsc: ENST00000542271.1:c.212T>A
  hgvsp: ENSP00000445616.1:p.Phe71Tyr
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000352069
  ensembl transcript: ENST00000359154
  gene symbol: WWP2
  hgvsc: ENST00000359154.2:c.560T>A
  hgvsp: ENSP00000352069.2:p.Phe187Tyr
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000396871
  ensembl transcript: ENST00000448661
  gene symbol: WWP2
  hgvsc: ENST00000448661.1:c.560T>A
  hgvsp: ENSP00000396871.1:p.Phe187Tyr
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000544162
  gene symbol: WWP2
  hgvsc: ENST00000544162.1:n.432T>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000455311
  ensembl transcript: ENST00000569174
  gene symbol: WWP2
  hgvsc: ENST00000569174.1:c.560T>A
  hgvsp: ENSP00000455311.1:p.Phe187Tyr
  variant of: http://identifiers.org/hgnc/16804
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6430
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8000
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29880
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9830
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2924
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1461
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35465
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Phe187Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

16-69876019-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69876019
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69876019
    reference: chr 16
allele count: 1
allele frequency: 9.943916312000319e-6
allele num: 100564
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000563618
  gene symbol: WWP2
  hgvsc: ENST00000563618.1:n.384T>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000348283
  ensembl transcript: ENST00000356003
  gene symbol: WWP2
  hgvsc: ENST00000356003.2:c.571T>A
  hgvsp: ENSP00000348283.2:p.Ser191Thr
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000455311
  ensembl transcript: ENST00000569174
  gene symbol: WWP2
  hgvsc: ENST00000569174.1:c.571T>A
  hgvsp: ENSP00000455311.1:p.Ser191Thr
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000567986
  gene symbol: WWP2
  hgvsc: ENST00000567986.1:n.481T>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000396871
  ensembl transcript: ENST00000448661
  gene symbol: WWP2
  hgvsc: ENST00000448661.1:c.571T>A
  hgvsp: ENSP00000396871.1:p.Ser191Thr
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000544162
  gene symbol: WWP2
  hgvsc: ENST00000544162.1:n.443T>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000352069
  ensembl transcript: ENST00000359154
  gene symbol: WWP2
  hgvsc: ENST00000359154.2:c.571T>A
  hgvsp: ENSP00000352069.2:p.Ser191Thr
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000445616
  ensembl transcript: ENST00000542271
  gene symbol: WWP2
  hgvsc: ENST00000542271.1:c.223T>A
  hgvsp: ENSP00000445616.1:p.Ser75Thr
  variant of: http://identifiers.org/hgnc/16804
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9349
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2685
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8570
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9461
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26060
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2602
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 802
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29979
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2074
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser191Thr
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/16-69876021-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69876021
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69876021
    reference: chr 16
allele count: 1
allele frequency: 1.003492152691366e-5
allele num: 99652
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000455311
  ensembl transcript: ENST00000569174
  gene symbol: WWP2
  hgvsc: ENST00000569174.1:c.573C>A
  hgvsp: ENST00000569174.1:c.573C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000567986
  gene symbol: WWP2
  hgvsc: ENST00000567986.1:n.483C>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000348283
  ensembl transcript: ENST00000356003
  gene symbol: WWP2
  hgvsc: ENST00000356003.2:c.573C>A
  hgvsp: ENST00000356003.2:c.573C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000352069
  ensembl transcript: ENST00000359154
  gene symbol: WWP2
  hgvsc: ENST00000359154.2:c.573C>A
  hgvsp: ENST00000359154.2:c.573C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000445616
  ensembl transcript: ENST00000542271
  gene symbol: WWP2
  hgvsc: ENST00000542271.1:c.225C>A
  hgvsp: ENST00000542271.1:c.225C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000396871
  ensembl transcript: ENST00000448661
  gene symbol: WWP2
  hgvsc: ENST00000448661.1:c.573C>A
  hgvsp: ENST00000448661.1:c.573C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000544162
  gene symbol: WWP2
  hgvsc: ENST00000544162.1:n.445C>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000563618
  gene symbol: WWP2
  hgvsc: ENST00000563618.1:n.386C>A
  variant of: http://identifiers.org/hgnc/16804
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2774
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9752
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8233
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9953
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25358
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28557
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2195
  bin: 2.75e1
  variant carriers: 0
hgvs: c.573C>A
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD

16-69876022-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69876022
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69876022
    reference: chr 16
allele count: 19
allele frequency: 1.910085250120637e-4
allele num: 99472
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000352069
  ensembl transcript: ENST00000359154
  gene symbol: WWP2
  hgvsc: ENST00000359154.2:c.574C>T
  hgvsp: ENSP00000352069.2:p.Arg192Trp
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000544162
  gene symbol: WWP2
  hgvsc: ENST00000544162.1:n.446C>T
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000396871
  ensembl transcript: ENST00000448661
  gene symbol: WWP2
  hgvsc: ENST00000448661.1:c.574C>T
  hgvsp: ENSP00000396871.1:p.Arg192Trp
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000348283
  ensembl transcript: ENST00000356003
  gene symbol: WWP2
  hgvsc: ENST00000356003.2:c.574C>T
  hgvsp: ENSP00000348283.2:p.Arg192Trp
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000445616
  ensembl transcript: ENST00000542271
  gene symbol: WWP2
  hgvsc: ENST00000542271.1:c.226C>T
  hgvsp: ENSP00000445616.1:p.Arg76Trp
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000567986
  gene symbol: WWP2
  hgvsc: ENST00000567986.1:n.484C>T
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000455311
  ensembl transcript: ENST00000569174
  gene symbol: WWP2
  hgvsc: ENST00000569174.1:c.574C>T
  hgvsp: ENSP00000455311.1:p.Arg192Trp
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000563618
  gene symbol: WWP2
  hgvsc: ENST00000563618.1:n.387C>T
  variant of: http://identifiers.org/hgnc/16804
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2681
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9969
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9776
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25369
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8259
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1115
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29094
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 557
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 731
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg192Trp
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

16-69876023-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69876023
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69876023
    reference: chr 16
allele count: 1
allele frequency: 1.006806008618259e-5
allele num: 99324
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000567986
  gene symbol: WWP2
  hgvsc: ENST00000567986.1:n.485G>T
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000352069
  ensembl transcript: ENST00000359154
  gene symbol: WWP2
  hgvsc: ENST00000359154.2:c.575G>T
  hgvsp: ENSP00000352069.2:p.Arg192Leu
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000396871
  ensembl transcript: ENST00000448661
  gene symbol: WWP2
  hgvsc: ENST00000448661.1:c.575G>T
  hgvsp: ENSP00000396871.1:p.Arg192Leu
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000348283
  ensembl transcript: ENST00000356003
  gene symbol: WWP2
  hgvsc: ENST00000356003.2:c.575G>T
  hgvsp: ENSP00000348283.2:p.Arg192Leu
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000455311
  ensembl transcript: ENST00000569174
  gene symbol: WWP2
  hgvsc: ENST00000569174.1:c.575G>T
  hgvsp: ENSP00000455311.1:p.Arg192Leu
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000563618
  gene symbol: WWP2
  hgvsc: ENST00000563618.1:n.388G>T
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000544162
  gene symbol: WWP2
  hgvsc: ENST00000544162.1:n.447G>T
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000445616
  ensembl transcript: ENST00000542271
  gene symbol: WWP2
  hgvsc: ENST00000542271.1:c.227G>T
  hgvsp: ENSP00000445616.1:p.Arg76Leu
  variant of: http://identifiers.org/hgnc/16804
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10002
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9856
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25353
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16029
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1063
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg192Leu
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/16-69876029-A-AC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69876029
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69876030
    reference: chr 16
allele count: 1
allele frequency: 1.039565877289644e-5
allele num: 96194
alternate allele: AC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000567986
  gene symbol: WWP2
  hgvsc: ENST00000567986.1:n.485+12dupC
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000455311
  ensembl transcript: ENST00000569174
  gene symbol: WWP2
  hgvsc: ENST00000569174.1:c.575+12dupC
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000348283
  ensembl transcript: ENST00000356003
  gene symbol: WWP2
  hgvsc: ENST00000356003.2:c.575+12dupC
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000396871
  ensembl transcript: ENST00000448661
  gene symbol: WWP2
  hgvsc: ENST00000448661.1:c.575+12dupC
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000352069
  ensembl transcript: ENST00000359154
  gene symbol: WWP2
  hgvsc: ENST00000359154.2:c.575+12dupC
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000445616
  ensembl transcript: ENST00000542271
  gene symbol: WWP2
  hgvsc: ENST00000542271.1:c.227+12dupC
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000563618
  gene symbol: WWP2
  hgvsc: ENST00000563618.1:n.388+12dupC
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000544162
  gene symbol: WWP2
  hgvsc: ENST00000544162.1:n.447+12dupC
  variant of: http://identifiers.org/hgnc/16804
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7667
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11052
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21464
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12931
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24910
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1286
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 668
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18766
  bin: 2.25e1
  variant carriers: 0
hgvs: c.575+12dupC
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/16-69876029-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69876029
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69876028
    reference: chr 16
allele count: 2
allele frequency: 2.079131754579288e-5
allele num: 96194
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000445616
  ensembl transcript: ENST00000542271
  gene symbol: WWP2
  hgvsc: ENST00000542271.1:c.227+12delC
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000563618
  gene symbol: WWP2
  hgvsc: ENST00000563618.1:n.388+12delC
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000544162
  gene symbol: WWP2
  hgvsc: ENST00000544162.1:n.447+12delC
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000396871
  ensembl transcript: ENST00000448661
  gene symbol: WWP2
  hgvsc: ENST00000448661.1:c.575+12delC
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000348283
  ensembl transcript: ENST00000356003
  gene symbol: WWP2
  hgvsc: ENST00000356003.2:c.575+12delC
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000567986
  gene symbol: WWP2
  hgvsc: ENST00000567986.1:n.485+12delC
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000352069
  ensembl transcript: ENST00000359154
  gene symbol: WWP2
  hgvsc: ENST00000359154.2:c.575+12delC
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000455311
  ensembl transcript: ENST00000569174
  gene symbol: WWP2
  hgvsc: ENST00000569174.1:c.575+12delC
  variant of: http://identifiers.org/hgnc/16804
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12931
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21464
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11052
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7667
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2736
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1103
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18766
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
hgvs: c.575+12delC
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: AC
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

16-69876031-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69876031
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69876031
    reference: chr 16
allele count: 2
allele frequency: 2.098768023170399e-5
allele num: 95294
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000352069
  ensembl transcript: ENST00000359154
  gene symbol: WWP2
  hgvsc: ENST00000359154.2:c.575+8C>G
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000445616
  ensembl transcript: ENST00000542271
  gene symbol: WWP2
  hgvsc: ENST00000542271.1:c.227+8C>G
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000396871
  ensembl transcript: ENST00000448661
  gene symbol: WWP2
  hgvsc: ENST00000448661.1:c.575+8C>G
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000348283
  ensembl transcript: ENST00000356003
  gene symbol: WWP2
  hgvsc: ENST00000356003.2:c.575+8C>G
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000563618
  gene symbol: WWP2
  hgvsc: ENST00000563618.1:n.388+8C>G
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000455311
  ensembl transcript: ENST00000569174
  gene symbol: WWP2
  hgvsc: ENST00000569174.1:c.575+8C>G
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000567986
  gene symbol: WWP2
  hgvsc: ENST00000567986.1:n.485+8C>G
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000544162
  gene symbol: WWP2
  hgvsc: ENST00000544162.1:n.447+8C>G
  variant of: http://identifiers.org/hgnc/16804
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2874
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20138
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11381
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13889
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2977
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1284
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 7.75e1
  variant carriers: 0
hgvs: c.575+8C>G
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/16-69876032-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69876032
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69876032
    reference: chr 16
allele count: 1
allele frequency: 1.051546825380134e-5
allele num: 95098
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000445616
  ensembl transcript: ENST00000542271
  gene symbol: WWP2
  hgvsc: ENST00000542271.1:c.227+9C>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000563618
  gene symbol: WWP2
  hgvsc: ENST00000563618.1:n.388+9C>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000396871
  ensembl transcript: ENST00000448661
  gene symbol: WWP2
  hgvsc: ENST00000448661.1:c.575+9C>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000352069
  ensembl transcript: ENST00000359154
  gene symbol: WWP2
  hgvsc: ENST00000359154.2:c.575+9C>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000544162
  gene symbol: WWP2
  hgvsc: ENST00000544162.1:n.447+9C>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000455311
  ensembl transcript: ENST00000569174
  gene symbol: WWP2
  hgvsc: ENST00000569174.1:c.575+9C>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000348283
  ensembl transcript: ENST00000356003
  gene symbol: WWP2
  hgvsc: ENST00000356003.2:c.575+9C>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000567986
  gene symbol: WWP2
  hgvsc: ENST00000567986.1:n.485+9C>A
  variant of: http://identifiers.org/hgnc/16804
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14431
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2801
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11591
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19552
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2161
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 643
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1295
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20196
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP

16-69876036-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69876036
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69876036
    reference: chr 16
allele count: 1
allele frequency: 1.069861987803573e-5
allele num: 93470
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000544162
  gene symbol: WWP2
  hgvsc: ENST00000544162.1:n.447+13T>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000352069
  ensembl transcript: ENST00000359154
  gene symbol: WWP2
  hgvsc: ENST00000359154.2:c.575+13T>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000445616
  ensembl transcript: ENST00000542271
  gene symbol: WWP2
  hgvsc: ENST00000542271.1:c.227+13T>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000455311
  ensembl transcript: ENST00000569174
  gene symbol: WWP2
  hgvsc: ENST00000569174.1:c.575+13T>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000567986
  gene symbol: WWP2
  hgvsc: ENST00000567986.1:n.485+13T>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000563618
  gene symbol: WWP2
  hgvsc: ENST00000563618.1:n.388+13T>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000396871
  ensembl transcript: ENST00000448661
  gene symbol: WWP2
  hgvsc: ENST00000448661.1:c.575+13T>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000348283
  ensembl transcript: ENST00000356003
  gene symbol: WWP2
  hgvsc: ENST00000356003.2:c.575+13T>A
  variant of: http://identifiers.org/hgnc/16804
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16305
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17226
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2091
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1101
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 696
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-48138032-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 48138032
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 48138032
    reference: chr 16
allele count: 2
allele frequency: 1.675912115168681e-5
allele num: 119338
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000434510
  ensembl transcript: ENST00000529084
  gene symbol: ABCC12
  hgvsc: ENST00000529084.1:c.*916+21C>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000437047
  ensembl transcript: ENST00000532494
  gene symbol: ABCC12
  hgvsc: ENST00000532494.1:c.2891+21C>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000413046
  ensembl transcript: ENST00000416054
  gene symbol: ABCC12
  hgvsc: ENST00000416054.1:c.*916+21C>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431354
  ensembl transcript: ENST00000534418
  gene symbol: ABCC12
  hgvsc: ENST00000534418.1:c.2654+21C>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000401855
  ensembl transcript: ENST00000448542
  gene symbol: ABCC12
  hgvsc: ENST00000448542.1:c.2664+1018C>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431232
  ensembl transcript: ENST00000497206
  gene symbol: ABCC12
  hgvsc: ENST00000497206.2:c.2891+21C>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000433333
  ensembl transcript: ENST00000529504
  gene symbol: ABCC12
  hgvsc: ENST00000529504.1:c.2664+1018C>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000311030
  ensembl transcript: ENST00000311303
  gene symbol: ABCC12
  hgvsc: ENST00000311303.3:c.2900+21C>A
  variant of: http://identifiers.org/hgnc/14640
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9348
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4218
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15164
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1134
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6371
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3701
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 694
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8385
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

16-48138046-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 48138046
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 48138046
    reference: chr 16
allele count: 9
allele frequency: 7.478934334956539e-5
allele num: 120338
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000311030
  ensembl transcript: ENST00000311303
  gene symbol: ABCC12
  hgvsc: ENST00000311303.3:c.2900+7C>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431232
  ensembl transcript: ENST00000497206
  gene symbol: ABCC12
  hgvsc: ENST00000497206.2:c.2891+7C>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000413046
  ensembl transcript: ENST00000416054
  gene symbol: ABCC12
  hgvsc: ENST00000416054.1:c.*916+7C>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000434510
  ensembl transcript: ENST00000529084
  gene symbol: ABCC12
  hgvsc: ENST00000529084.1:c.*916+7C>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431354
  ensembl transcript: ENST00000534418
  gene symbol: ABCC12
  hgvsc: ENST00000534418.1:c.2654+7C>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000437047
  ensembl transcript: ENST00000532494
  gene symbol: ABCC12
  hgvsc: ENST00000532494.1:c.2891+7C>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000433333
  ensembl transcript: ENST00000529504
  gene symbol: ABCC12
  hgvsc: ENST00000529504.1:c.2664+1004C>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000401855
  ensembl transcript: ENST00000448542
  gene symbol: ABCC12
  hgvsc: ENST00000448542.1:c.2664+1004C>A
  variant of: http://identifiers.org/hgnc/14640
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4286
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15958
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9807
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23634
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28051
  bin: 6.25e1
  variant carriers: 0
hgvs: c.2900+7C>A
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD

16-48138047-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 48138047
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 48138047
    reference: chr 16
allele count: 2
allele frequency: 1.661101975050248e-5
allele num: 120402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000434510
  ensembl transcript: ENST00000529084
  gene symbol: ABCC12
  hgvsc: ENST00000529084.1:c.*916+6C>G
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431232
  ensembl transcript: ENST00000497206
  gene symbol: ABCC12
  hgvsc: ENST00000497206.2:c.2891+6C>G
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431354
  ensembl transcript: ENST00000534418
  gene symbol: ABCC12
  hgvsc: ENST00000534418.1:c.2654+6C>G
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000413046
  ensembl transcript: ENST00000416054
  gene symbol: ABCC12
  hgvsc: ENST00000416054.1:c.*916+6C>G
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000433333
  ensembl transcript: ENST00000529504
  gene symbol: ABCC12
  hgvsc: ENST00000529504.1:c.2664+1003C>G
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000437047
  ensembl transcript: ENST00000532494
  gene symbol: ABCC12
  hgvsc: ENST00000532494.1:c.2891+6C>G
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000311030
  ensembl transcript: ENST00000311303
  gene symbol: ABCC12
  hgvsc: ENST00000311303.3:c.2900+6C>G
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000401855
  ensembl transcript: ENST00000448542
  gene symbol: ABCC12
  hgvsc: ENST00000448542.1:c.2664+1003C>G
  variant of: http://identifiers.org/hgnc/14640
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23607
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9843
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4296
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15989
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6411
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
hgvs: c.2900+6C>G
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

16-48138047-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 48138047
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 48138047
    reference: chr 16
allele count: 1
allele frequency: 8.305509875251242e-6
allele num: 120402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000437047
  ensembl transcript: ENST00000532494
  gene symbol: ABCC12
  hgvsc: ENST00000532494.1:c.2891+6C>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000434510
  ensembl transcript: ENST00000529084
  gene symbol: ABCC12
  hgvsc: ENST00000529084.1:c.*916+6C>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000433333
  ensembl transcript: ENST00000529504
  gene symbol: ABCC12
  hgvsc: ENST00000529504.1:c.2664+1003C>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000401855
  ensembl transcript: ENST00000448542
  gene symbol: ABCC12
  hgvsc: ENST00000448542.1:c.2664+1003C>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000413046
  ensembl transcript: ENST00000416054
  gene symbol: ABCC12
  hgvsc: ENST00000416054.1:c.*916+6C>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000311030
  ensembl transcript: ENST00000311303
  gene symbol: ABCC12
  hgvsc: ENST00000311303.3:c.2900+6C>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431354
  ensembl transcript: ENST00000534418
  gene symbol: ABCC12
  hgvsc: ENST00000534418.1:c.2654+6C>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431232
  ensembl transcript: ENST00000497206
  gene symbol: ABCC12
  hgvsc: ENST00000497206.2:c.2891+6C>A
  variant of: http://identifiers.org/hgnc/14640
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23607
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15989
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4296
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3839
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
hgvs: c.2900+6C>A
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

16-48138050-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 48138050
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 48138050
    reference: chr 16
allele count: 1
allele frequency: 8.293386853323161e-6
allele num: 120578
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431354
  ensembl transcript: ENST00000534418
  gene symbol: ABCC12
  hgvsc: ENST00000534418.1:c.2654+3A>C
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000401855
  ensembl transcript: ENST00000448542
  gene symbol: ABCC12
  hgvsc: ENST00000448542.1:c.2664+1000A>C
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000311030
  ensembl transcript: ENST00000311303
  gene symbol: ABCC12
  hgvsc: ENST00000311303.3:c.2900+3A>C
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000437047
  ensembl transcript: ENST00000532494
  gene symbol: ABCC12
  hgvsc: ENST00000532494.1:c.2891+3A>C
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000434510
  ensembl transcript: ENST00000529084
  gene symbol: ABCC12
  hgvsc: ENST00000529084.1:c.*916+3A>C
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431232
  ensembl transcript: ENST00000497206
  gene symbol: ABCC12
  hgvsc: ENST00000497206.2:c.2891+3A>C
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000433333
  ensembl transcript: ENST00000529504
  gene symbol: ABCC12
  hgvsc: ENST00000529504.1:c.2664+1000A>C
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000413046
  ensembl transcript: ENST00000416054
  gene symbol: ABCC12
  hgvsc: ENST00000416054.1:c.*916+3A>C
  variant of: http://identifiers.org/hgnc/14640
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9902
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4301
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16089
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3875
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1716
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
hgvs: c.2900+3A>C
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-48138053-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 48138053
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 48138053
    reference: chr 16
allele count: 3
allele frequency: 2.485007123687088e-5
allele num: 120724
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000434510
  ensembl transcript: ENST00000529084
  gene symbol: ABCC12
  hgvsc: ENST00000529084.1:c.*916G>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431354
  ensembl transcript: ENST00000534418
  gene symbol: ABCC12
  hgvsc: ENST00000534418.1:c.2654G>A
  hgvsp: ENSP00000431354.1:p.Arg885His
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000401855
  ensembl transcript: ENST00000448542
  gene symbol: ABCC12
  hgvsc: ENST00000448542.1:c.2664+997G>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000413046
  ensembl transcript: ENST00000416054
  gene symbol: ABCC12
  hgvsc: ENST00000416054.1:c.*916G>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000437047
  ensembl transcript: ENST00000532494
  gene symbol: ABCC12
  hgvsc: ENST00000532494.1:c.2891G>A
  hgvsp: ENSP00000437047.1:p.Arg964His
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000311030
  ensembl transcript: ENST00000311303
  gene symbol: ABCC12
  hgvsc: ENST00000311303.3:c.2900G>A
  hgvsp: ENSP00000311030.3:p.Arg967His
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431232
  ensembl transcript: ENST00000497206
  gene symbol: ABCC12
  hgvsc: ENST00000497206.2:c.2891G>A
  hgvsp: ENSP00000431232.1:p.Arg964His
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000433333
  ensembl transcript: ENST00000529504
  gene symbol: ABCC12
  hgvsc: ENST00000529504.1:c.2664+997G>A
  variant of: http://identifiers.org/hgnc/14640
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9987
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16187
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23601
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4325
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28346
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg967His
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

16-48138054-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 48138054
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 48138054
    reference: chr 16
allele count: 3
allele frequency: 2.483608185972581e-5
allele num: 120792
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431232
  ensembl transcript: ENST00000497206
  gene symbol: ABCC12
  hgvsc: ENST00000497206.2:c.2890C>T
  hgvsp: ENSP00000431232.1:p.Arg964Cys
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000434510
  ensembl transcript: ENST00000529084
  gene symbol: ABCC12
  hgvsc: ENST00000529084.1:c.*915C>T
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431354
  ensembl transcript: ENST00000534418
  gene symbol: ABCC12
  hgvsc: ENST00000534418.1:c.2653C>T
  hgvsp: ENSP00000431354.1:p.Arg885Cys
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000437047
  ensembl transcript: ENST00000532494
  gene symbol: ABCC12
  hgvsc: ENST00000532494.1:c.2890C>T
  hgvsp: ENSP00000437047.1:p.Arg964Cys
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000401855
  ensembl transcript: ENST00000448542
  gene symbol: ABCC12
  hgvsc: ENST00000448542.1:c.2664+996C>T
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000413046
  ensembl transcript: ENST00000416054
  gene symbol: ABCC12
  hgvsc: ENST00000416054.1:c.*915C>T
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000433333
  ensembl transcript: ENST00000529504
  gene symbol: ABCC12
  hgvsc: ENST00000529504.1:c.2664+996C>T
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000311030
  ensembl transcript: ENST00000311303
  gene symbol: ABCC12
  hgvsc: ENST00000311303.3:c.2899C>T
  hgvsp: ENSP00000311030.3:p.Arg967Cys
  variant of: http://identifiers.org/hgnc/14640
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23612
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10013
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16238
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4328
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3742
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1721
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4814
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg967Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

16-69876045-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69876045
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69876045
    reference: chr 16
allele count: 63
allele frequency: 7.046979865771812e-4
allele num: 89400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000348283
  ensembl transcript: ENST00000356003
  gene symbol: WWP2
  hgvsc: ENST00000356003.2:c.575+22A>T
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000544162
  gene symbol: WWP2
  hgvsc: ENST00000544162.1:n.447+22A>T
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000445616
  ensembl transcript: ENST00000542271
  gene symbol: WWP2
  hgvsc: ENST00000542271.1:c.227+22A>T
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000352069
  ensembl transcript: ENST00000359154
  gene symbol: WWP2
  hgvsc: ENST00000359154.2:c.575+22A>T
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000563618
  gene symbol: WWP2
  hgvsc: ENST00000563618.1:n.388+22A>T
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000455311
  ensembl transcript: ENST00000569174
  gene symbol: WWP2
  hgvsc: ENST00000569174.1:c.575+22A>T
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000396871
  ensembl transcript: ENST00000448661
  gene symbol: WWP2
  hgvsc: ENST00000448661.1:c.575+22A>T
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000567986
  gene symbol: WWP2
  hgvsc: ENST00000567986.1:n.485+22A>T
  variant of: http://identifiers.org/hgnc/16804
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13303
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3903
  bin: 1.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 11345
  bin: 2.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 5376
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21004
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1686
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 586
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 675
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2154
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1792
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1158
  bin: 9.75e1
  variant carriers: 60
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 695
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4980
  bin: 3.25e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum

16-69876060-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69876060
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69876060
    reference: chr 16
allele count: 2
allele frequency: 2.432498175626368e-5
allele num: 82220
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000455311
  ensembl transcript: ENST00000569174
  gene symbol: WWP2
  hgvsc: ENST00000569174.1:c.575+37G>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000396871
  ensembl transcript: ENST00000448661
  gene symbol: WWP2
  hgvsc: ENST00000448661.1:c.575+37G>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000348283
  ensembl transcript: ENST00000356003
  gene symbol: WWP2
  hgvsc: ENST00000356003.2:c.575+37G>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000352069
  ensembl transcript: ENST00000359154
  gene symbol: WWP2
  hgvsc: ENST00000359154.2:c.575+37G>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000544162
  gene symbol: WWP2
  hgvsc: ENST00000544162.1:n.447+37G>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000567986
  gene symbol: WWP2
  hgvsc: ENST00000567986.1:n.485+37G>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000563618
  gene symbol: WWP2
  hgvsc: ENST00000563618.1:n.388+37G>A
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000445616
  ensembl transcript: ENST00000542271
  gene symbol: WWP2
  hgvsc: ENST00000542271.1:c.227+37G>A
  variant of: http://identifiers.org/hgnc/16804
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21781
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8433
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15098
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3868
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1249
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1054
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2104
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1099
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 5476
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21365
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4486
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1337
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum

16-69876069-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69876069
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69876069
    reference: chr 16
allele count: 2
allele frequency: 2.627913699314115e-5
allele num: 76106
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000544162
  gene symbol: WWP2
  hgvsc: ENST00000544162.1:n.447+46A>G
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000563618
  gene symbol: WWP2
  hgvsc: ENST00000563618.1:n.388+46A>G
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000455311
  ensembl transcript: ENST00000569174
  gene symbol: WWP2
  hgvsc: ENST00000569174.1:c.575+46A>G
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000445616
  ensembl transcript: ENST00000542271
  gene symbol: WWP2
  hgvsc: ENST00000542271.1:c.227+46A>G
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000352069
  ensembl transcript: ENST00000359154
  gene symbol: WWP2
  hgvsc: ENST00000359154.2:c.575+46A>G
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000396871
  ensembl transcript: ENST00000448661
  gene symbol: WWP2
  hgvsc: ENST00000448661.1:c.575+46A>G
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl transcript: ENST00000567986
  gene symbol: WWP2
  hgvsc: ENST00000567986.1:n.485+46A>G
  variant of: http://identifiers.org/hgnc/16804
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198373
  ensembl protein: ENSP00000348283
  ensembl transcript: ENST00000356003
  gene symbol: WWP2
  hgvsc: ENST00000356003.2:c.575+46A>G
  variant of: http://identifiers.org/hgnc/16804
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4551
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4025
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17931
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19306
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9002
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1659
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17008
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4997
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5413
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP

16-48138055-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 48138055
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 48138055
    reference: chr 16
allele count: 3
allele frequency: 2.482128673550437e-5
allele num: 120864
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000433333
  ensembl transcript: ENST00000529504
  gene symbol: ABCC12
  hgvsc: ENST00000529504.1:c.2664+995A>C
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000437047
  ensembl transcript: ENST00000532494
  gene symbol: ABCC12
  hgvsc: ENST00000532494.1:c.2889A>C
  hgvsp: ENSP00000437047.1:p.Leu963Phe
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431232
  ensembl transcript: ENST00000497206
  gene symbol: ABCC12
  hgvsc: ENST00000497206.2:c.2889A>C
  hgvsp: ENSP00000431232.1:p.Leu963Phe
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000311030
  ensembl transcript: ENST00000311303
  gene symbol: ABCC12
  hgvsc: ENST00000311303.3:c.2898A>C
  hgvsp: ENSP00000311030.3:p.Leu966Phe
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000413046
  ensembl transcript: ENST00000416054
  gene symbol: ABCC12
  hgvsc: ENST00000416054.1:c.*914A>C
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000434510
  ensembl transcript: ENST00000529084
  gene symbol: ABCC12
  hgvsc: ENST00000529084.1:c.*914A>C
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000401855
  ensembl transcript: ENST00000448542
  gene symbol: ABCC12
  hgvsc: ENST00000448542.1:c.2664+995A>C
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431354
  ensembl transcript: ENST00000534418
  gene symbol: ABCC12
  hgvsc: ENST00000534418.1:c.2652A>C
  hgvsp: ENSP00000431354.1:p.Leu884Phe
  variant of: http://identifiers.org/hgnc/14640
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16263
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4328
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu966Phe
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
reference allele: T
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

16-48138057-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 48138057
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 48138057
    reference: chr 16
allele count: 2
allele frequency: 1.653904040487571e-5
allele num: 120926
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000311030
  ensembl transcript: ENST00000311303
  gene symbol: ABCC12
  hgvsc: ENST00000311303.3:c.2896T>A
  hgvsp: ENSP00000311030.3:p.Leu966Ile
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000434510
  ensembl transcript: ENST00000529084
  gene symbol: ABCC12
  hgvsc: ENST00000529084.1:c.*912T>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000437047
  ensembl transcript: ENST00000532494
  gene symbol: ABCC12
  hgvsc: ENST00000532494.1:c.2887T>A
  hgvsp: ENSP00000437047.1:p.Leu963Ile
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000433333
  ensembl transcript: ENST00000529504
  gene symbol: ABCC12
  hgvsc: ENST00000529504.1:c.2664+993T>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431232
  ensembl transcript: ENST00000497206
  gene symbol: ABCC12
  hgvsc: ENST00000497206.2:c.2887T>A
  hgvsp: ENSP00000431232.1:p.Leu963Ile
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000413046
  ensembl transcript: ENST00000416054
  gene symbol: ABCC12
  hgvsc: ENST00000416054.1:c.*912T>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000401855
  ensembl transcript: ENST00000448542
  gene symbol: ABCC12
  hgvsc: ENST00000448542.1:c.2664+993T>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431354
  ensembl transcript: ENST00000534418
  gene symbol: ABCC12
  hgvsc: ENST00000534418.1:c.2650T>A
  hgvsp: ENSP00000431354.1:p.Leu884Ile
  variant of: http://identifiers.org/hgnc/14640
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10015
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4332
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16288
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23679
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8842
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu966Ile
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

16-48138063-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 48138063
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 48138063
    reference: chr 16
allele count: 1
allele frequency: 8.260366760284156e-6
allele num: 121060
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000311030
  ensembl transcript: ENST00000311303
  gene symbol: ABCC12
  hgvsc: ENST00000311303.3:c.2890A>G
  hgvsp: ENSP00000311030.3:p.Ile964Val
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000437047
  ensembl transcript: ENST00000532494
  gene symbol: ABCC12
  hgvsc: ENST00000532494.1:c.2881A>G
  hgvsp: ENSP00000437047.1:p.Ile961Val
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000401855
  ensembl transcript: ENST00000448542
  gene symbol: ABCC12
  hgvsc: ENST00000448542.1:c.2664+987A>G
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431232
  ensembl transcript: ENST00000497206
  gene symbol: ABCC12
  hgvsc: ENST00000497206.2:c.2881A>G
  hgvsp: ENSP00000431232.1:p.Ile961Val
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000433333
  ensembl transcript: ENST00000529504
  gene symbol: ABCC12
  hgvsc: ENST00000529504.1:c.2664+987A>G
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000434510
  ensembl transcript: ENST00000529084
  gene symbol: ABCC12
  hgvsc: ENST00000529084.1:c.*906A>G
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000413046
  ensembl transcript: ENST00000416054
  gene symbol: ABCC12
  hgvsc: ENST00000416054.1:c.*906A>G
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431354
  ensembl transcript: ENST00000534418
  gene symbol: ABCC12
  hgvsc: ENST00000534418.1:c.2644A>G
  hgvsp: ENSP00000431354.1:p.Ile882Val
  variant of: http://identifiers.org/hgnc/14640
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16355
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23698
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4338
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10052
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3917
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4836
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile964Val
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/16-48138090-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 48138090
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 48138090
    reference: chr 16
allele count: 6
allele frequency: 4.944131316127757e-5
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431232
  ensembl transcript: ENST00000497206
  gene symbol: ABCC12
  hgvsc: ENST00000497206.2:c.2854G>T
  hgvsp: ENSP00000431232.1:p.Val952Leu
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000413046
  ensembl transcript: ENST00000416054
  gene symbol: ABCC12
  hgvsc: ENST00000416054.1:c.*879G>T
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000437047
  ensembl transcript: ENST00000532494
  gene symbol: ABCC12
  hgvsc: ENST00000532494.1:c.2854G>T
  hgvsp: ENSP00000437047.1:p.Val952Leu
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000401855
  ensembl transcript: ENST00000448542
  gene symbol: ABCC12
  hgvsc: ENST00000448542.1:c.2664+960G>T
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000311030
  ensembl transcript: ENST00000311303
  gene symbol: ABCC12
  hgvsc: ENST00000311303.3:c.2863G>T
  hgvsp: ENSP00000311030.3:p.Val955Leu
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000434510
  ensembl transcript: ENST00000529084
  gene symbol: ABCC12
  hgvsc: ENST00000529084.1:c.*879G>T
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000433333
  ensembl transcript: ENST00000529504
  gene symbol: ABCC12
  hgvsc: ENST00000529504.1:c.2664+960G>T
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431354
  ensembl transcript: ENST00000534418
  gene symbol: ABCC12
  hgvsc: ENST00000534418.1:c.2617G>T
  hgvsp: ENSP00000431354.1:p.Val873Leu
  variant of: http://identifiers.org/hgnc/14640
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10114
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16497
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6435
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 2100
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val955Leu
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff

16-48138090-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 48138090
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 48138090
    reference: chr 16
allele count: 3
allele frequency: 2.472065658063878e-5
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431232
  ensembl transcript: ENST00000497206
  gene symbol: ABCC12
  hgvsc: ENST00000497206.2:c.2854G>A
  hgvsp: ENSP00000431232.1:p.Val952Met
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000434510
  ensembl transcript: ENST00000529084
  gene symbol: ABCC12
  hgvsc: ENST00000529084.1:c.*879G>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431354
  ensembl transcript: ENST00000534418
  gene symbol: ABCC12
  hgvsc: ENST00000534418.1:c.2617G>A
  hgvsp: ENSP00000431354.1:p.Val873Met
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000401855
  ensembl transcript: ENST00000448542
  gene symbol: ABCC12
  hgvsc: ENST00000448542.1:c.2664+960G>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000433333
  ensembl transcript: ENST00000529504
  gene symbol: ABCC12
  hgvsc: ENST00000529504.1:c.2664+960G>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000437047
  ensembl transcript: ENST00000532494
  gene symbol: ABCC12
  hgvsc: ENST00000532494.1:c.2854G>A
  hgvsp: ENSP00000437047.1:p.Val952Met
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000413046
  ensembl transcript: ENST00000416054
  gene symbol: ABCC12
  hgvsc: ENST00000416054.1:c.*879G>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000311030
  ensembl transcript: ENST00000311303
  gene symbol: ABCC12
  hgvsc: ENST00000311303.3:c.2863G>A
  hgvsp: ENSP00000311030.3:p.Val955Met
  variant of: http://identifiers.org/hgnc/14640
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10114
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16497
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3766
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1731
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6435
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val955Met
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-48138091-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 48138091
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 48138091
    reference: chr 16
allele count: 2
allele frequency: 1.647935137272997e-5
allele num: 121364
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000311030
  ensembl transcript: ENST00000311303
  gene symbol: ABCC12
  hgvsc: ENST00000311303.3:c.2862C>T
  hgvsp: ENST00000311303.3:c.2862C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000413046
  ensembl transcript: ENST00000416054
  gene symbol: ABCC12
  hgvsc: ENST00000416054.1:c.*878C>T
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431354
  ensembl transcript: ENST00000534418
  gene symbol: ABCC12
  hgvsc: ENST00000534418.1:c.2616C>T
  hgvsp: ENST00000534418.1:c.2616C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000433333
  ensembl transcript: ENST00000529504
  gene symbol: ABCC12
  hgvsc: ENST00000529504.1:c.2664+959C>T
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000437047
  ensembl transcript: ENST00000532494
  gene symbol: ABCC12
  hgvsc: ENST00000532494.1:c.2853C>T
  hgvsp: ENST00000532494.1:c.2853C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000401855
  ensembl transcript: ENST00000448542
  gene symbol: ABCC12
  hgvsc: ENST00000448542.1:c.2664+959C>T
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431232
  ensembl transcript: ENST00000497206
  gene symbol: ABCC12
  hgvsc: ENST00000497206.2:c.2853C>T
  hgvsp: ENST00000497206.2:c.2853C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000434510
  ensembl transcript: ENST00000529084
  gene symbol: ABCC12
  hgvsc: ENST00000529084.1:c.*878C>T
  variant of: http://identifiers.org/hgnc/14640
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16500
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28920
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6431
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Val954Val
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

16-48138099-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 48138099
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 48138099
    reference: chr 16
allele count: 2
allele frequency: 1.647717910693689e-5
allele num: 121380
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431354
  ensembl transcript: ENST00000534418
  gene symbol: ABCC12
  hgvsc: ENST00000534418.1:c.2608C>G
  hgvsp: ENSP00000431354.1:p.Leu870Val
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000413046
  ensembl transcript: ENST00000416054
  gene symbol: ABCC12
  hgvsc: ENST00000416054.1:c.*870C>G
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431232
  ensembl transcript: ENST00000497206
  gene symbol: ABCC12
  hgvsc: ENST00000497206.2:c.2845C>G
  hgvsp: ENSP00000431232.1:p.Leu949Val
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000433333
  ensembl transcript: ENST00000529504
  gene symbol: ABCC12
  hgvsc: ENST00000529504.1:c.2664+951C>G
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000437047
  ensembl transcript: ENST00000532494
  gene symbol: ABCC12
  hgvsc: ENST00000532494.1:c.2845C>G
  hgvsp: ENSP00000437047.1:p.Leu949Val
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000434510
  ensembl transcript: ENST00000529084
  gene symbol: ABCC12
  hgvsc: ENST00000529084.1:c.*870C>G
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000311030
  ensembl transcript: ENST00000311303
  gene symbol: ABCC12
  hgvsc: ENST00000311303.3:c.2854C>G
  hgvsp: ENSP00000311030.3:p.Leu952Val
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000401855
  ensembl transcript: ENST00000448542
  gene symbol: ABCC12
  hgvsc: ENST00000448542.1:c.2664+951C>G
  variant of: http://identifiers.org/hgnc/14640
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23700
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16508
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1731
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6431
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu952Val
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

16-48138101-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 48138101
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 48138101
    reference: chr 16
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431232
  ensembl transcript: ENST00000497206
  gene symbol: ABCC12
  hgvsc: ENST00000497206.2:c.2843T>C
  hgvsp: ENSP00000431232.1:p.Val948Ala
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431354
  ensembl transcript: ENST00000534418
  gene symbol: ABCC12
  hgvsc: ENST00000534418.1:c.2606T>C
  hgvsp: ENSP00000431354.1:p.Val869Ala
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000311030
  ensembl transcript: ENST00000311303
  gene symbol: ABCC12
  hgvsc: ENST00000311303.3:c.2852T>C
  hgvsp: ENSP00000311030.3:p.Val951Ala
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000413046
  ensembl transcript: ENST00000416054
  gene symbol: ABCC12
  hgvsc: ENST00000416054.1:c.*868T>C
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000437047
  ensembl transcript: ENST00000532494
  gene symbol: ABCC12
  hgvsc: ENST00000532494.1:c.2843T>C
  hgvsp: ENSP00000437047.1:p.Val948Ala
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000401855
  ensembl transcript: ENST00000448542
  gene symbol: ABCC12
  hgvsc: ENST00000448542.1:c.2664+949T>C
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000433333
  ensembl transcript: ENST00000529504
  gene symbol: ABCC12
  hgvsc: ENST00000529504.1:c.2664+949T>C
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000434510
  ensembl transcript: ENST00000529084
  gene symbol: ABCC12
  hgvsc: ENST00000529084.1:c.*868T>C
  variant of: http://identifiers.org/hgnc/14640
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23700
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3767
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6431
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Val951Ala
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ

16-48138105-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 48138105
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 48138105
    reference: chr 16
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000437047
  ensembl transcript: ENST00000532494
  gene symbol: ABCC12
  hgvsc: ENST00000532494.1:c.2839G>A
  hgvsp: ENSP00000437047.1:p.Ala947Thr
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000434510
  ensembl transcript: ENST00000529084
  gene symbol: ABCC12
  hgvsc: ENST00000529084.1:c.*864G>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000413046
  ensembl transcript: ENST00000416054
  gene symbol: ABCC12
  hgvsc: ENST00000416054.1:c.*864G>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431354
  ensembl transcript: ENST00000534418
  gene symbol: ABCC12
  hgvsc: ENST00000534418.1:c.2602G>A
  hgvsp: ENSP00000431354.1:p.Ala868Thr
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431232
  ensembl transcript: ENST00000497206
  gene symbol: ABCC12
  hgvsc: ENST00000497206.2:c.2839G>A
  hgvsp: ENSP00000431232.1:p.Ala947Thr
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000311030
  ensembl transcript: ENST00000311303
  gene symbol: ABCC12
  hgvsc: ENST00000311303.3:c.2848G>A
  hgvsp: ENSP00000311030.3:p.Ala950Thr
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000401855
  ensembl transcript: ENST00000448542
  gene symbol: ABCC12
  hgvsc: ENST00000448542.1:c.2664+945G>A
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000433333
  ensembl transcript: ENST00000529504
  gene symbol: ABCC12
  hgvsc: ENST00000529504.1:c.2664+945G>A
  variant of: http://identifiers.org/hgnc/14640
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4358
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10126
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23692
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3767
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6433
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala950Thr
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

16-48138111-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 48138111
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 48138111
    reference: chr 16
allele count: 10
allele frequency: 8.237639422047218e-5
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000433333
  ensembl transcript: ENST00000529504
  gene symbol: ABCC12
  hgvsc: ENST00000529504.1:c.2664+939T>C
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431354
  ensembl transcript: ENST00000534418
  gene symbol: ABCC12
  hgvsc: ENST00000534418.1:c.2596T>C
  hgvsp: ENSP00000431354.1:p.Phe866Leu
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000413046
  ensembl transcript: ENST00000416054
  gene symbol: ABCC12
  hgvsc: ENST00000416054.1:c.*858T>C
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000434510
  ensembl transcript: ENST00000529084
  gene symbol: ABCC12
  hgvsc: ENST00000529084.1:c.*858T>C
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000437047
  ensembl transcript: ENST00000532494
  gene symbol: ABCC12
  hgvsc: ENST00000532494.1:c.2833T>C
  hgvsp: ENSP00000437047.1:p.Phe945Leu
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000311030
  ensembl transcript: ENST00000311303
  gene symbol: ABCC12
  hgvsc: ENST00000311303.3:c.2842T>C
  hgvsp: ENSP00000311030.3:p.Phe948Leu
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000401855
  ensembl transcript: ENST00000448542
  gene symbol: ABCC12
  hgvsc: ENST00000448542.1:c.2664+939T>C
  variant of: http://identifiers.org/hgnc/14640
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140798
  ensembl protein: ENSP00000431232
  ensembl transcript: ENST00000497206
  gene symbol: ABCC12
  hgvsc: ENST00000497206.2:c.2833T>C
  hgvsp: ENSP00000431232.1:p.Phe945Leu
  variant of: http://identifiers.org/hgnc/14640
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23689
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16518
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2100
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3767
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Phe948Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum

GenotypeQuality
all individuals: 249
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33587
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2121
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11058
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2507
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13890
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51984
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6680
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 770
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.039567611666327e-4
allele num: 9806
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5980
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.872e0

FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.325385e6

QD
type: SiteQuality
SIO_000300: 1.906e1

MQRankSum
type: SiteQuality
SIO_000300: 2.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.6e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.47e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 2749
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58486
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.316482359136387e-4
allele num: 7596
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9244
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10496
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6246
num of homozygotes: 0

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

QD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

MQ
type: SiteQuality
SIO_000300: 5.938e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.91e-1

VQSLOD
type: SiteQuality
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MQRankSum
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SIO_000300: 1.61e0

ReadPosRankSum
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SIO_000300: 1.34e0

DP
type: SiteQuality
SIO_000300: 1.438606e6

FS
type: SiteQuality
SIO_000300: 3.619e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.562e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
allele num: 9388
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 10592
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.67549091883922e-5
allele num: 59684
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6282
num of homozygotes: 0

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

FS
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SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: 5.01e0

VQSLOD
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MQ
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SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.53e-1

InbreedingCoeff
type: SiteQuality
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MQRankSum
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SIO_000300: 7.32e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.39e-1

QD
type: SiteQuality
SIO_000300: 1.446e1

DP
type: SiteQuality
SIO_000300: 1.455682e6

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

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

Latino
type: Population
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allele frequency: 0.0e0
allele num: 10592
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.626027034190299e-5
allele num: 15092
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.446e1

MQRankSum
type: SiteQuality
SIO_000300: 7.32e-1

DP
type: SiteQuality
SIO_000300: 1.455682e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 5.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.39e-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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variant carriers: 0

Latino
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allele frequency: 0.0e0
allele num: 11126
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.848335631278314e-5
allele num: 10154
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64848
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.225099601593625e-5
allele num: 16064
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6464
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
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QD
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SIO_000300: 1.575e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.44e-1

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

MQRankSum
type: SiteQuality
SIO_000300: -1.18e-1

DP
type: SiteQuality
SIO_000300: 1.540376e6

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8494
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10302
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.868393047179851e-5
allele num: 11276
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6506
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16246
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65710
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.016e1

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -9.9e-2

MQRankSum
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.62e-1

DP
type: SiteQuality
SIO_000300: 1.556087e6

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 902
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East Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66308
num of homozygotes: 0

South Asian
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allele frequency: 6.093102607847916e-5
allele num: 16412
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.152e1

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.883e1

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
type: Population
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allele frequency: 0.0e0
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Latino
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allele num: 11410
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South Asian
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6552
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DP
type: SiteQuality
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ReadPosRankSum
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VQSLOD
type: SiteQuality
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InbreedingCoeff
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QD
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele frequency: 4.52106817770812e-5
allele num: 66356
num of homozygotes: 0

Latino
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allele num: 11420
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

African
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East Asian
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South Asian
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Other
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MQRankSum
type: SiteQuality
SIO_000300: 4.2e-1

VQSLOD
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QD
type: SiteQuality
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FS
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 16430
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 2.887947631882942e-4
allele num: 10388
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66376
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6552
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Latino
type: Population
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Other
type: Population
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allele num: 902
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DP
type: SiteQuality
SIO_000300: 1.570374e6

MQRankSum
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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QD
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3220
bin: 9.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.92492781520693e-4
allele num: 10390
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66376
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16434
num of homozygotes: 0

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

ClippingRankSum
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SIO_000300: 1.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.304e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.12e0

VQSLOD
type: SiteQuality
SIO_000300: 8.090000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.570385e6

FS
type: SiteQuality
SIO_000300: 3.079e0

MQRankSum
type: SiteQuality
SIO_000300: 1.89e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.02e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506704836522525e-5
allele num: 66370
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16434
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.1e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.467e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.793e0

DP
type: SiteQuality
SIO_000300: 1.570227e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.326e0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16432
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.519705917801615e-5
allele num: 66376
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.92492781520693e-4
allele num: 10390
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.974e1

MQRankSum
type: SiteQuality
SIO_000300: -5.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.769e0

VQSLOD
type: SiteQuality
SIO_000300: 2.19e0

FS
type: SiteQuality
SIO_000300: 5.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.35e-1

QD
type: SiteQuality
SIO_000300: 1.046e1

DP
type: SiteQuality
SIO_000300: 1.570649e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506614035616356e-5
allele num: 66374
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16436
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.178e0

VQSLOD
type: SiteQuality
SIO_000300: -1.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.36e-1

QD
type: SiteQuality
SIO_000300: 5.4e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.92e-1

DP
type: SiteQuality
SIO_000300: 1.570686e6

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.013863773357444e-5
allele num: 66360
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.88e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.32e-1

FS
type: SiteQuality
SIO_000300: 3.548e0

MQ
type: SiteQuality
SIO_000300: 5.919e1

QD
type: SiteQuality
SIO_000300: 7.98e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.513e0

DP
type: SiteQuality
SIO_000300: 1.571104e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.4e-2

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66356
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.088650754992694e-5
allele num: 16424
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.571102e6

MQRankSum
type: SiteQuality
SIO_000300: -1.93e-1

QD
type: SiteQuality
SIO_000300: 1.121e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.3e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.569e-1

FS
type: SiteQuality
SIO_000300: 4.747e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.106e0

MQ
type: SiteQuality
SIO_000300: 5.886e1

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
all individuals: 778
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66352
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.090133982947625e-5
allele num: 16420
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11424
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 5.932e1

MQRankSum
type: SiteQuality
SIO_000300: 7.0e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 8.82e-1

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 9.75e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.19e-1

DP
type: SiteQuality
SIO_000300: 1.570358e6

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11424
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507386192342478e-5
allele num: 66340
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.570067e6

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.86e1

InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -5.94e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.28e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 7.53e0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66320
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6564
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South Asian
type: Population
allele count: 0
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Other
type: Population
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allele frequency: 0.0e0
allele num: 902
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11410
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African
type: Population
allele count: 1
allele frequency: 9.63020030816641e-5
allele num: 10384
num of homozygotes: 0

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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FS
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.524669146795145e-5
allele num: 65588
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.168e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.4e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.45e0

DP
type: SiteQuality
SIO_000300: 1.54699e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.56e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.224e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 153
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 809
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3217
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 705
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2821
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 46388
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10250
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11222
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.183151916706105e-4
allele num: 8452
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16120
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65178
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.529439e6

MQ
type: SiteQuality
SIO_000300: 5.948e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.01e0

QD
type: SiteQuality
SIO_000300: 1.212e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.3e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.181e0

MQRankSum
type: SiteQuality
SIO_000300: 2.51e0

GenotypeQuality
all individuals: 113
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1870
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 752
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 632
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35055
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2506
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10920
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.578681485223541e-5
allele num: 63344
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.4330900243309e-4
allele num: 8220
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15736
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6442
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10044
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

MQRankSum
type: SiteQuality
SIO_000300: 3.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.21e-1

FS
type: SiteQuality
SIO_000300: 1.573e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e0

DP
type: SiteQuality
SIO_000300: 1.441031e6

QD
type: SiteQuality
SIO_000300: 5.47e0

GenotypeQuality
all individuals: 74
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2703
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3639
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3217
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 643
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6444
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.577287066246057e-5
allele num: 63400
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: 8208
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10062
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15774
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.619e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.53e-1

DP
type: SiteQuality
SIO_000300: 1.419181e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

VQSLOD
type: SiteQuality
SIO_000300: -9.19e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.22e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.6e0

GenotypeQuality
all individuals: 704
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2336
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2448
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2848
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3216
bin: 9.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63200
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6434
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10032
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.157509157509158e-5
allele num: 10920
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8182
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15742
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.91e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.83e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.344e0

QD
type: SiteQuality
SIO_000300: 6.05e0

VQSLOD
type: SiteQuality
SIO_000300: -1.118e0

DP
type: SiteQuality
SIO_000300: 1.411653e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 2429
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8073
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32111
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 7.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8172
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10020
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10912
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63098
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6438
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.357279084551812e-5
allele num: 15730
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.74e0

MQRankSum
type: SiteQuality
SIO_000300: -5.32e-1

FS
type: SiteQuality
SIO_000300: 3.926e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.05e-1

DP
type: SiteQuality
SIO_000300: 1.400781e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.22e0

QD
type: SiteQuality
SIO_000300: 1.372e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

GenotypeQuality
all individuals: 5201
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28849
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2280
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3507
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15682
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6424
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10004
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8144
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10872
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.590027348470394e-5
allele num: 62892
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.06e0

MQRankSum
type: SiteQuality
SIO_000300: -8.33e-1

QD
type: SiteQuality
SIO_000300: 1.66e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.53e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.479e-1

DP
type: SiteQuality
SIO_000300: 1.373007e6

GenotypeQuality
all individuals: 392
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26543
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 604
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1040
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2282
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6414
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10856
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9990
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8130
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.593625498007968e-5
allele num: 62750
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.21e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 9.1e-1

QD
type: SiteQuality
SIO_000300: 1.054e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.21e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.353412e6

GenotypeQuality
all individuals: 1993
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22093
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9085
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1674
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4960
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1225
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3239
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 175
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8098
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15586
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.203485392106612e-5
allele num: 62432
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6402
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10806
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.457e1

FS
type: SiteQuality
SIO_000300: 1.654e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-2

DP
type: SiteQuality
SIO_000300: 1.330853e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.91e0

VQSLOD
type: SiteQuality
SIO_000300: 3.71e0

GenotypeQuality
all individuals: 603
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22093
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 227
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1225
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 242
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4960
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1674
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6402
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10806
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62432
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8098
num of homozygotes: 0

South Asian
type: Population
allele count: 28
allele frequency: 1.796484024124214e-3
allele num: 15586
num of homozygotes: 1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-2

FS
type: SiteQuality
SIO_000300: 1.654e0

DP
type: SiteQuality
SIO_000300: 1.330853e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

QD
type: SiteQuality
SIO_000300: 1.457e1

VQSLOD
type: SiteQuality
SIO_000300: 3.71e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.91e0

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.39e-1

GenotypeQuality
all individuals: 7797
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2640
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6848
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1486
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3222
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 387
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variant carriers: 0

GenotypeQuality
all individuals: 2782
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15418
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8000
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61672
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 9.146341463414635e-4
allele num: 9840
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10708
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6364
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.72e-1

QD
type: SiteQuality
SIO_000300: 1.434e1

MQRankSum
type: SiteQuality
SIO_000300: 4.15e-1

DP
type: SiteQuality
SIO_000300: 1.291628e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

FS
type: SiteQuality
SIO_000300: 1.668e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.053e0

VQSLOD
type: SiteQuality
SIO_000300: 2.3e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 615
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1645
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4458
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16753
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2644
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6370
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9856
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61728
num of homozygotes: 0

East Asian
type: Population
allele count: 11
allele frequency: 1.373283395755306e-3
allele num: 8010
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10718
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15406
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -3.9e-2

FS
type: SiteQuality
SIO_000300: 1.271e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.33e0

DP
type: SiteQuality
SIO_000300: 1.289422e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.2e-2

QD
type: SiteQuality
SIO_000300: 1.439e1

VQSLOD
type: SiteQuality
SIO_000300: 3.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.27e-1

GenotypeQuality
all individuals: 43
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42082
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 473
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3365
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 972
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 970
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7060
bin: 2.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5974
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8374
num of homozygotes: 0

African
type: Population
allele count: 26
allele frequency: 2.932551319648094e-3
allele num: 8866
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14928
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.89000189000189e-4
allele num: 10582
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.716593343855997e-5
allele num: 59554
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.129999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.314457e6

VQSLOD
type: SiteQuality
SIO_000300: 5.83e0

QD
type: SiteQuality
SIO_000300: 1.362e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 545
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7722
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 564
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 962
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3265
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 780
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 844
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14846
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10540
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8808
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5940
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.692276450280918e-5
allele num: 59092
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.67e-1

QD
type: SiteQuality
SIO_000300: 7.5e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

MQ
type: SiteQuality
SIO_000300: 5.714e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.67e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.558e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.84e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.115e0

DP
type: SiteQuality
SIO_000300: 1.303213e6

GenotypeQuality
all individuals: 490
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 901
bin: 7.75e1
variant carriers: 3

GenotypeQuality
all individuals: 8053
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1569
bin: 9.75e1
variant carriers: 474

GenotypeQuality
all individuals: 264
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 454
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 520
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 460
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 909
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 260
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 777
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 526
bin: 8.25e1
variant carriers: 2

South Asian
type: Population
allele count: 13
allele frequency: 8.775482651545835e-4
allele num: 14814
num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 5.037783375314861e-3
allele num: 794
num of homozygotes: 0

Latino
type: Population
allele count: 11
allele frequency: 1.04602510460251e-3
allele num: 10516
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 48
allele frequency: 8.061807188444743e-3
allele num: 5954
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8342
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 6.83371298405467e-4
allele num: 8780
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 406
allele frequency: 6.894677852121047e-3
allele num: 58886
num of homozygotes: 3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e-1

DP
type: SiteQuality
SIO_000300: 1.306363e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.176e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.76e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.97e-1

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

GenotypeQuality
all individuals: 886
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3160
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 893
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 917
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8476
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40522
bin: 6.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58554
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 5.710370031978072e-4
allele num: 8756
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14794
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8324
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5948
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

DP
type: SiteQuality
SIO_000300: 1.296018e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.070000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

MQRankSum
type: SiteQuality
SIO_000300: -4.34e-1

QD
type: SiteQuality
SIO_000300: 1.208e1

FS
type: SiteQuality
SIO_000300: 2.776e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.271e0

GenotypeQuality
all individuals: 1104
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 495
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1016
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 856
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3074
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 1.265822784810127e-3
allele num: 790
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10440
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5890
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.720637324064834e-5
allele num: 58118
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8292
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8702
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14752
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.399999999999999e-1

QD
type: SiteQuality
SIO_000300: 7.06e0

VQSLOD
type: SiteQuality
SIO_000300: -1.525e0

MQRankSum
type: SiteQuality
SIO_000300: 1.4e0

MQ
type: SiteQuality
SIO_000300: 5.911e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

FS
type: SiteQuality
SIO_000300: 4.449e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.72e-1

DP
type: SiteQuality
SIO_000300: 1.285993e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.18e-1

GenotypeQuality
all individuals: 257
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38561
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1126
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9924
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 515
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variant carriers: 0

GenotypeQuality
all individuals: 1103
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 257
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 850
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.739553978359949e-5
allele num: 57486
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5844
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8256
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14666
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.3e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.75e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.268507e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.099e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.1e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

QD
type: SiteQuality
SIO_000300: 9.76e0

GenotypeQuality
all individuals: 172
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
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variant carriers: 0

GenotypeQuality
all individuals: 7759
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1067
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variant carriers: 0

GenotypeQuality
all individuals: 6786
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 242
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GenotypeQuality
all individuals: 17210
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 523
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2642
bin: 4.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15356
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9822
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7978
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6364
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.356287425149701e-5
allele num: 10688
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61484
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.177e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.11e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.33e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.17e0

QD
type: SiteQuality
SIO_000300: 1.164e1

DP
type: SiteQuality
SIO_000300: 1.289376e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.11e-1

GenotypeQuality
all individuals: 9147
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1591
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1053
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 7897
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 383
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 585
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2829
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 7073
bin: 3.75e1
variant carriers: 1

African
type: Population
allele count: 229
allele frequency: 2.331975560081466e-2
allele num: 9820
num of homozygotes: 3

Other
type: Population
allele count: 1
allele frequency: 1.152073732718894e-3
allele num: 868
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15368
num of homozygotes: 0

Latino
type: Population
allele count: 10
allele frequency: 9.351037965214139e-4
allele num: 10694
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7976
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6364
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.625540492213661e-5
allele num: 61518
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.284879e6

MQRankSum
type: SiteQuality
SIO_000300: 1.89e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.01e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.693e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.66e0

GenotypeQuality
all individuals: 3700
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 243
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variant carriers: 0

GenotypeQuality
all individuals: 1299
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7630
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6272
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59246
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.65513110608279e-5
allele num: 15026
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.747e1

QD
type: SiteQuality
SIO_000300: 1.066e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.199e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.37e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.656e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.350000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

DP
type: SiteQuality
SIO_000300: 1.258418e6

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2061
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9772
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.365400702693659e-5
allele num: 11954
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6386
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7552
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10588
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60222
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.37e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.05e0

QD
type: SiteQuality
SIO_000300: 2.296e1

DP
type: SiteQuality
SIO_000300: 1.408967e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.182e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.07e-1

GenotypeQuality
all individuals: 830
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 90
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variant carriers: 0

GenotypeQuality
all individuals: 1501
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56116
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.685503685503685e-4
allele num: 8140
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5738
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14478
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.43e0

MQRankSum
type: SiteQuality
SIO_000300: -1.45e-1

DP
type: SiteQuality
SIO_000300: 1.232726e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.61e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.44e-1

QD
type: SiteQuality
SIO_000300: 1.44e1

GenotypeQuality
all individuals: 774
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1152
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 519
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14168
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8152
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53972
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.784439685938615e-4
allele num: 5604
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9986
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.936e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -4.905e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.39e-1

QD
type: SiteQuality
SIO_000300: 9.119999999999999e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.8e-1

DP
type: SiteQuality
SIO_000300: 1.168496e6

GenotypeQuality
all individuals: 1101
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 755
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 15809
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 222
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variant carriers: 0

GenotypeQuality
all individuals: 843
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8072
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9918
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14106
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7872
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.87336080929187e-5
allele num: 53380
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.05e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.155156e6

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

FS
type: SiteQuality
SIO_000300: 2.96e0

QD
type: SiteQuality
SIO_000300: 1.252e1

GenotypeQuality
all individuals: 15868
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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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: 3.25e1
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
all individuals: 1119
bin: 9.75e1
variant carriers: 19

South Asian
type: Population
allele count: 10
allele frequency: 7.098239636570131e-4
allele num: 14088
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 3.026634382566586e-4
allele num: 9912
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5538
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8050
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7856
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 9.38297552919982e-5
allele num: 53288
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.351351351351351e-3
allele num: 740
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.9e-2

FS
type: SiteQuality
SIO_000300: 1.452e0

QD
type: SiteQuality
SIO_000300: 1.257e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.28e0

MQRankSum
type: SiteQuality
SIO_000300: 2.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.155468e6

GenotypeQuality
all individuals: 219
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 624
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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
all individuals: 255
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GenotypeQuality
all individuals: 1102
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 713
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variant carriers: 0

GenotypeQuality
all individuals: 29618
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 894
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variant carriers: 0

GenotypeQuality
all individuals: 2423
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9910
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14080
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53154
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.27420998980632e-4
allele num: 7848
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5542
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8050
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.19e-1

DP
type: SiteQuality
SIO_000300: 1.15446e6

MQRankSum
type: SiteQuality
SIO_000300: 6.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.614e0

VQSLOD
type: SiteQuality
SIO_000300: -6.212e-1

FS
type: SiteQuality
SIO_000300: 6.659e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e-1

GenotypeQuality
all individuals: 438
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2206
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 745
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
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GenotypeQuality
all individuals: 249
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1103
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 250
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variant carriers: 0

GenotypeQuality
all individuals: 216
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GenotypeQuality
all individuals: 2806
bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13828
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7618
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 724
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5422
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.951143370014829e-5
allele num: 51252
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7794
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.8e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

DP
type: SiteQuality
SIO_000300: 1.097108e6

FS
type: SiteQuality
SIO_000300: 7.533e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.19e0

QD
type: SiteQuality
SIO_000300: 8.039999999999999e0

MQ
type: SiteQuality
SIO_000300: 6.039e1

GenotypeQuality
all individuals: 24910
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 745
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 752
bin: 5.25e1
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GenotypeQuality
all individuals: 713
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GenotypeQuality
all individuals: 1189
bin: 7.5e0
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GenotypeQuality
all individuals: 668
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GenotypeQuality
all individuals: 250
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 4.75e1
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GenotypeQuality
all individuals: 1286
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2806
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 482
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2206
bin: 6.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7618
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7794
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5422
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.38121546961326e-3
allele num: 724
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.951143370014829e-5
allele num: 51252
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

DP
type: SiteQuality
SIO_000300: 1.097108e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.37e-1

FS
type: SiteQuality
SIO_000300: 7.533e0

MQ
type: SiteQuality
SIO_000300: 6.039e1

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.19e0

QD
type: SiteQuality
SIO_000300: 8.039999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.8e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13752
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9460
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.323101349563376e-4
allele num: 7558
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 50700
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.396648044692737e-3
allele num: 716
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

DP
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SIO_000300: 1.080483e6

BaseQRankSum
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SIO_000300: 1.03e0

MQRankSum
type: SiteQuality
SIO_000300: 3.17e-1

MQ
type: SiteQuality
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VQSLOD
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FS
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SIO_000300: 3.197e0

QD
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SIO_000300: 1.21e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.97e-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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variant carriers: 1

South Asian
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allele count: 1
allele frequency: 7.289692374981776e-5
allele num: 13718
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7722
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 50586
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7530
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5396
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 716
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9430
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.75e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

QD
type: SiteQuality
SIO_000300: 1.53e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.206e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.96e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.070246e6

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7412
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7598
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9250
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.017674831524152e-5
allele num: 49562
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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allele count: 0
allele frequency: 0.0e0
allele num: 712
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5350
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.0353e6

QD
type: SiteQuality
SIO_000300: 1.19e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -8.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.599999999999999e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.93e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.791e0

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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bin: 9.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.749781277340332e-4
allele num: 11430
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10270
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65528
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16322
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8326
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.136e1

VQSLOD
type: SiteQuality
SIO_000300: 9.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.99e-1

FS
type: SiteQuality
SIO_000300: 2.344e0

DP
type: SiteQuality
SIO_000300: 1.716083e6

MQRankSum
type: SiteQuality
SIO_000300: 3.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.255e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.820000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.932e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 9

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.362109150346581e-4
allele num: 66074
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8458
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.38e-1

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.361e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

FS
type: SiteQuality
SIO_000300: 3.55e0

DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66122
num of homozygotes: 0

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

East Asian
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allele frequency: 2.362948960302458e-4
allele num: 8464
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

African
type: Population
allele count: 0
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.06e-1

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.748112e6

GenotypeQuality
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variant carriers: 0

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

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

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
type: Population
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allele num: 898
num of homozygotes: 0

Latino
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num of homozygotes: 0

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

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

Latino
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allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.177856301531213e-4
allele num: 8490
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66236
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 902
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InbreedingCoeff
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QD
type: SiteQuality
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MQRankSum
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MQ
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DP
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FS
type: SiteQuality
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

South Asian
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allele count: 2
allele frequency: 1.21300339640951e-4
allele num: 16488
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.648784253184099e-5
allele num: 10364
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66322
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.755494e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.3e-1

FS
type: SiteQuality
SIO_000300: 1.535e0

VQSLOD
type: SiteQuality
SIO_000300: 3.52e0

MQRankSum
type: SiteQuality
SIO_000300: 4.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.55e-1

QD
type: SiteQuality
SIO_000300: 1.402e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

GenotypeQuality
all individuals: 49
bin: 4.75e1
variant carriers: 0

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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bin: 9.25e1
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.52106817770812e-5
allele num: 66356
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.38e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.756773e6

QD
type: SiteQuality
SIO_000300: 1.29e1

FS
type: SiteQuality
SIO_000300: 1.387e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.53e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.04e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13294
num of homozygotes: 0

East Asian
type: Population
allele count: 62
allele frequency: 8.781869688385268e-3
allele num: 7060
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7324
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.457725947521866e-3
allele num: 686
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5174
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8798
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47064
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.6e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.15e1

VQSLOD
type: SiteQuality
SIO_000300: 4.62e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.33e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-3

DP
type: SiteQuality
SIO_000300: 9.41191e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.33e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 198
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.700573469963335e-5
allele num: 42548
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4818
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12710
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6806
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8234
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6474
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

QD
type: SiteQuality
SIO_000300: 1.421e1

FS
type: SiteQuality
SIO_000300: 9.173e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.599999999999999e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.099999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.33e-1

DP
type: SiteQuality
SIO_000300: 8.39201e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.36e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1206
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12276
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5910
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6318
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.149065444621801e-5
allele num: 38842
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7662
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 584
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

MQRankSum
type: SiteQuality
SIO_000300: -2.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.19e-2

FS
type: SiteQuality
SIO_000300: 2.569e0

QD
type: SiteQuality
SIO_000300: 1.528e1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 8.07654e5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.513703443429375e-4
allele num: 8538
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66404
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.3842e1

QD
type: SiteQuality
SIO_000300: 1.541e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.99e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.895e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.72e0

VQSLOD
type: SiteQuality
SIO_000300: -2.119e0

DP
type: SiteQuality
SIO_000300: 1.757583e6

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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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.010053578953705e-5
allele num: 66444
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8546
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.442e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.758308e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.324e0

VQSLOD
type: SiteQuality
SIO_000300: 8.06e-1

QD
type: SiteQuality
SIO_000300: 1.497e1

FS
type: SiteQuality
SIO_000300: 2.544e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.101e0

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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variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503307276007216e-5
allele num: 66520
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.958e1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.4e-1

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.89e-1

DP
type: SiteQuality
SIO_000300: 1.76063e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 6
allele frequency: 5.184033177812338e-4
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66704
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.2e-2

DP
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.686e0

VQSLOD
type: SiteQuality
SIO_000300: 9.1e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e-1

FS
type: SiteQuality
SIO_000300: 9.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8916
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4843
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28911
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499160470136723e-5
allele num: 66704
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.178e1

FS
type: SiteQuality
SIO_000300: 9.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.765615e6

VQSLOD
type: SiteQuality
SIO_000300: 9.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.686e0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2101
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 4.75e-1

QD
type: SiteQuality
SIO_000300: 1.434e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.37e0

DP
type: SiteQuality
SIO_000300: 1.765592e6

FS
type: SiteQuality
SIO_000300: 9.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 7.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.96e0

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

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 28940
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997601918465228e-5
allele num: 66720
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.5e-1

FS
type: SiteQuality
SIO_000300: 2.853e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.62e-1

MQ
type: SiteQuality
SIO_000300: 5.941e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -7.54e-1

QD
type: SiteQuality
SIO_000300: 1.452e1

MQRankSum
type: SiteQuality
SIO_000300: 1.25e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e0

DP
type: SiteQuality
SIO_000300: 1.765882e6

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 8919
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 3930
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4846
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variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.98e0

DP
type: SiteQuality
SIO_000300: 1.76568e6

FS
type: SiteQuality
SIO_000300: 5.518e0

MQRankSum
type: SiteQuality
SIO_000300: 8.120000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

QD
type: SiteQuality
SIO_000300: 1.268e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.29e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

GenotypeQuality
all individuals: 1732
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 2101
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 4847
bin: 7.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: -3.1e-2

FS
type: SiteQuality
SIO_000300: 1.6481e1

VQSLOD
type: SiteQuality
SIO_000300: -2.324e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.57e-1

QD
type: SiteQuality
SIO_000300: 1.366e1

MQ
type: SiteQuality
SIO_000300: 5.982e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.3e0

DP
type: SiteQuality
SIO_000300: 1.76592e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.962e0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6442
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variant carriers: 10

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 8922
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 3933
bin: 7.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.498666187093487e-4
allele num: 66726
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 2.86e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.68e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.975e1

MQRankSum
type: SiteQuality
SIO_000300: -1.06e-1