13-100523144-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523144
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523144
    reference: chr 13
allele count: 0
allele frequency: 0.0e0
allele num: 112548
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.701-48A>G
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.92-48A>G
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.701-48A>G
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.701-48A>G
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.803-48A>G
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.803-48A>G
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6374
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3015
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2354
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2587
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3984
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5509
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7066
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4935
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2399
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 921
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1674
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 963
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1744
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2539
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2812
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

13-100523148-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523148
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523148
    reference: chr 13
allele count: 1
allele frequency: 8.88525580651467e-6
allele num: 112546
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.701-44C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.701-44C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.92-44C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.803-44C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.701-44C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.803-44C>T
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5511
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2353
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7072
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7269
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3992
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6374
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2587
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4935
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2412
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2033
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 934
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1678
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 629
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2530
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2404
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

13-100523153-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523153
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523153
    reference: chr 13
allele count: 5
allele frequency: 4.441128401904356e-5
allele num: 112584
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.701-39C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.701-39C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.803-39C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.803-39C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.92-39C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.701-39C>T
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4009
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2353
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4935
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6374
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5521
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3509
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7269
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7074
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2587
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2810
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.25e1
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genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2414
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD

13-100523154-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523154
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523154
    reference: chr 13
allele count: 2
allele frequency: 1.77421357983074e-5
allele num: 112726
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.92-38G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.803-38G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.701-38G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.803-38G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.701-38G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.701-38G>A
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2353
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6308
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3509
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4017
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4935
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7071
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2587
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1678
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 875
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37601
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2419
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2406
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

13-100523161-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523161
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523161
    reference: chr 13
allele count: 45
allele frequency: 3.988159597284506e-4
allele num: 112834
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.701-31C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.803-31C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.92-31C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.803-31C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.701-31C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.701-31C>T
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6380
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 4045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5518
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2586
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6307
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 7066
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7263
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3513
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4937
  bin: 5.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1417
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4263
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37617
  bin: 9.75e1
  variant carriers: 47
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 1.25e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP

13-100523162-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523162
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523162
    reference: chr 13
allele count: 156
allele frequency: 1.38109318837757e-3
allele num: 112954
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.701-30G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.92-30G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.803-30G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.803-30G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.701-30G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.701-30G>A
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 6.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4049
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7059
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7248
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6300
  bin: 5.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 9.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5526
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4930
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 6377
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 7.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 2604
  bin: 9.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 7.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 8.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 478
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 686
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 37605
  bin: 9.75e1
  variant carriers: 154
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4287
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1420
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2997
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 2
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

13-100523169-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523169
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523169
    reference: chr 13
allele count: 8
allele frequency: 7.061772858076019e-5
allele num: 113286
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.803-23C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.803-23C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.701-23C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.92-23C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.701-23C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.701-23C>T
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6299
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4938
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7070
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5530
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6380
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2416
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37572
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 1677
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1430
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2447
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4437
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

13-100523170-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523170
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523170
    reference: chr 13
allele count: 8
allele frequency: 7.052559197418764e-5
allele num: 113434
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.701-22G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.803-22G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.803-22G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.701-22G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.92-22G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.701-22G>A
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6379
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3485
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6299
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5531
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4938
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7069
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7258
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3503
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2531
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1676
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1432
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2416
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3346
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2451
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

13-100523172-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523172
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523172
    reference: chr 13
allele count: 3
allele frequency: 2.6398690624945e-5
allele num: 113642
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.701-20T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.701-20T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.701-20T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.92-20T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.803-20T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.803-20T>C
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3480
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7070
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5530
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6380
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2416
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3416
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4655
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2461
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37569
  bin: 9.75e1
  variant carriers: 3
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

13-100523177-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523177
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523177
    reference: chr 13
allele count: 2
allele frequency: 1.755063357787216e-5
allele num: 113956
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.92-15T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.701-15T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.803-15T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.701-15T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.803-15T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.701-15T>C
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3503
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4091
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7256
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6380
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7071
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5535
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4940
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2421
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2470
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3400
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2539
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

13-100523182-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523182
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523182
    reference: chr 13
allele count: 2
allele frequency: 1.748740906547286e-5
allele num: 114368
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.92-10A>G
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.803-10A>G
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.701-10A>G
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.701-10A>G
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.803-10A>G
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.701-10A>G
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4940
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7071
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3502
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6301
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6380
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5536
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37570
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.25e1
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2483
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genotype quality: GenotypeQuality
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  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2423
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3266
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP

13-100523183-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523183
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523183
    reference: chr 13
allele count: 1
allele frequency: 8.734845043848922e-6
allele num: 114484
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.701-9T>G
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.92-9T>G
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.701-9T>G
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.803-9T>G
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.803-9T>G
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.701-9T>G
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6380
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1978
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5536
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6301
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7071
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3503
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3242
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2538
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1446
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1677
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff

13-100523202-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523202
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523202
    reference: chr 13
allele count: 1
allele frequency: 8.529221111528095e-6
allele num: 117244
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.813G>A
  hgvsp: ENST00000376360.1:c.813G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.711G>A
  hgvsp: ENST00000376354.1:c.711G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.102G>A
  hgvsp: ENST00000419700.1:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.813G>A
  hgvsp: ENST00000339105.4:c.813G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.711G>A
  hgvsp: ENST00000444838.2:c.711G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.711G>A
  hgvsp: ENST00000376355.3:c.711G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3503
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4336
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5564
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4940
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2001
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6381
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7071
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37570
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2639
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2094
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6359
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val271Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

13-100523208-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523208
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523208
    reference: chr 13
allele count: 1
allele frequency: 8.469838903664053e-6
allele num: 118066
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.717C>T
  hgvsp: ENST00000444838.2:c.717C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.108C>T
  hgvsp: ENST00000419700.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.717C>T
  hgvsp: ENST00000376355.3:c.717C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.819C>T
  hgvsp: ENST00000339105.4:c.819C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.717C>T
  hgvsp: ENST00000376354.1:c.717C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.819C>T
  hgvsp: ENST00000376360.1:c.819C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4476
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7071
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6383
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3503
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4940
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6301
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1686
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2579
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2815
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 4.75e1
  variant carriers: 0
hgvs: p.His273His
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

13-100523210-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523210
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523210
    reference: chr 13
allele count: 1
allele frequency: 8.444234276835777e-6
allele num: 118424
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.719C>G
  hgvsp: ENSP00000365532.1:p.Pro240Arg
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.719C>G
  hgvsp: ENSP00000365533.3:p.Pro240Arg
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.719C>G
  hgvsp: ENSP00000404768.2:p.Pro240Arg
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.821C>G
  hgvsp: ENSP00000342991.4:p.Pro274Arg
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.110C>G
  hgvsp: ENSP00000396574.1:p.Pro37Arg
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.821C>G
  hgvsp: ENSP00000365538.1:p.Pro274Arg
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6386
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4942
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4548
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6301
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3757
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3503
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7072
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1499
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2732
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2501
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro274Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

13-100523223-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523223
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523223
    reference: chr 13
allele count: 25
allele frequency: 2.087368913232249e-4
allele num: 119768
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.732C>T
  hgvsp: ENST00000444838.2:c.732C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.732C>T
  hgvsp: ENST00000376355.3:c.732C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.732C>T
  hgvsp: ENST00000376354.1:c.732C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.123C>T
  hgvsp: ENST00000419700.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.834C>T
  hgvsp: ENST00000376360.1:c.834C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.834C>T
  hgvsp: ENST00000339105.4:c.834C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4936
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4209
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2586
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5737
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6394
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6302
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7070
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4867
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3503
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2831
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1706
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7298
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala278Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ

13-100523231-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523231
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523231
    reference: chr 13
allele count: 1
allele frequency: 8.299995020002988e-6
allele num: 120482
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.740A>G
  hgvsp: ENSP00000365533.3:p.Gln247Arg
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.131A>G
  hgvsp: ENSP00000396574.1:p.Gln44Arg
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.740A>G
  hgvsp: ENSP00000365532.1:p.Gln247Arg
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.740A>G
  hgvsp: ENSP00000404768.2:p.Gln247Arg
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.842A>G
  hgvsp: ENSP00000342991.4:p.Gln281Arg
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.842A>G
  hgvsp: ENSP00000365538.1:p.Gln281Arg
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7071
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4938
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3505
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6304
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2641
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2841
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1641
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7659
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gln281Arg
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

13-100523243-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523243
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523243
    reference: chr 13
allele count: 1
allele frequency: 8.27348843366317e-6
allele num: 120868
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.752C>G
  hgvsp: ENSP00000404768.2:p.Ser251Cys
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.752C>G
  hgvsp: ENSP00000365532.1:p.Ser251Cys
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.854C>G
  hgvsp: ENSP00000342991.4:p.Ser285Cys
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.143C>G
  hgvsp: ENSP00000396574.1:p.Ser48Cys
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.854C>G
  hgvsp: ENSP00000365538.1:p.Ser285Cys
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.752C>G
  hgvsp: ENSP00000365533.3:p.Ser251Cys
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3505
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5867
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5214
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4552
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6412
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7079
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4937
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7808
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2844
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3031
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1672
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1721
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser285Cys
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD

http://identifiers.org/exac.variant/13-100523245-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523245
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523245
    reference: chr 13
allele count: 5
allele frequency: 4.13517045172602e-5
allele num: 120914
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.856C>A
  hgvsp: ENSP00000365538.1:p.Pro286Thr
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.754C>A
  hgvsp: ENSP00000365532.1:p.Pro252Thr
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.754C>A
  hgvsp: ENSP00000365533.3:p.Pro252Thr
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.754C>A
  hgvsp: ENSP00000404768.2:p.Pro252Thr
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.856C>A
  hgvsp: ENSP00000342991.4:p.Pro286Thr
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.145C>A
  hgvsp: ENSP00000396574.1:p.Pro49Thr
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4554
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3505
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5241
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4937
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7077
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2651
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2666
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37581
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 3040
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7880
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1681
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro286Thr
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

13-100523252-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523252
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523252
    reference: chr 13
allele count: 1
allele frequency: 8.259684480052863e-6
allele num: 121070
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.863C>G
  hgvsp: ENSP00000342991.4:p.Pro288Arg
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.152C>G
  hgvsp: ENSP00000396574.1:p.Pro51Arg
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.761C>G
  hgvsp: ENSP00000404768.2:p.Pro254Arg
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.761C>G
  hgvsp: ENSP00000365532.1:p.Pro254Arg
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.761C>G
  hgvsp: ENSP00000365533.3:p.Pro254Arg
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.863C>G
  hgvsp: ENSP00000365538.1:p.Pro288Arg
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4937
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5953
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7078
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2676
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2848
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2679
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3090
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1718
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro288Arg
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

13-100523253-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523253
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523253
    reference: chr 13
allele count: 1
allele frequency: 8.257365570088519e-6
allele num: 121104
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.864T>G
  hgvsp: ENST00000376360.1:c.864T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.864T>G
  hgvsp: ENST00000339105.4:c.864T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.762T>G
  hgvsp: ENST00000444838.2:c.762T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.153T>G
  hgvsp: ENST00000419700.1:c.153T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.762T>G
  hgvsp: ENST00000376355.3:c.762T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.762T>G
  hgvsp: ENST00000376354.1:c.762T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7076
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4937
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5313
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4549
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6307
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2687
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3097
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8000
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro288Pro
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum

13-100523254-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523254
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523255
    reference: chr 13
allele count: 2
allele frequency: 1.651200422707308e-5
allele num: 121124
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.769dupA
  hgvsp: ENSP00000404768.2:p.Ile257AsnfsTer2
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.160dupA
  hgvsp: ENSP00000396574.1:p.Ile54AsnfsTer2
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.871dupA
  hgvsp: ENSP00000365538.1:p.Ile291AsnfsTer2
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.769dupA
  hgvsp: ENSP00000365533.3:p.Ile257AsnfsTer2
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.871dupA
  hgvsp: ENSP00000342991.4:p.Ile291AsnfsTer2
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.769dupA
  hgvsp: ENSP00000365532.1:p.Ile257AsnfsTer2
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7076
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6424
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4936
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5965
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2688
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1692
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ile291AsnfsTer2
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

13-100523256-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523256
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523256
    reference: chr 13
allele count: 1
allele frequency: 8.253821519363466e-6
allele num: 121156
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.765A>G
  hgvsp: ENST00000376355.3:c.765A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.765A>G
  hgvsp: ENST00000444838.2:c.765A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.156A>G
  hgvsp: ENST00000419700.1:c.156A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.867A>G
  hgvsp: ENST00000376360.1:c.867A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.765A>G
  hgvsp: ENST00000376354.1:c.765A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.867A>G
  hgvsp: ENST00000339105.4:c.867A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6421
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5333
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5970
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4937
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7075
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1693
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2851
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu289Glu
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

13-100523261-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523261
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523261
    reference: chr 13
allele count: 1
allele frequency: 8.251233559417133e-6
allele num: 121194
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.872T>C
  hgvsp: ENSP00000342991.4:p.Ile291Thr
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.770T>C
  hgvsp: ENSP00000365533.3:p.Ile257Thr
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.161T>C
  hgvsp: ENSP00000396574.1:p.Ile54Thr
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.770T>C
  hgvsp: ENSP00000365532.1:p.Ile257Thr
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.872T>C
  hgvsp: ENSP00000365538.1:p.Ile291Thr
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.770T>C
  hgvsp: ENSP00000404768.2:p.Ile257Thr
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6421
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5978
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7075
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4937
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1692
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2683
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37582
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8087
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile291Thr
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

13-100523268-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523268
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523268
    reference: chr 13
allele count: 1
allele frequency: 8.247966876165026e-6
allele num: 121242
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.879G>C
  hgvsp: ENSP00000365538.1:p.Trp293Cys
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.777G>C
  hgvsp: ENSP00000365532.1:p.Trp259Cys
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.777G>C
  hgvsp: ENSP00000404768.2:p.Trp259Cys
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.777G>C
  hgvsp: ENSP00000365533.3:p.Trp259Cys
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.168G>C
  hgvsp: ENSP00000396574.1:p.Trp56Cys
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.879G>C
  hgvsp: ENSP00000342991.4:p.Trp293Cys
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7077
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6428
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5998
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4565
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5377
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4937
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1721
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3125
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2681
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1696
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Trp293Cys
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD

13-100523271-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523271
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523271
    reference: chr 13
allele count: 2
allele frequency: 1.649511744523621e-5
allele num: 121248
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.171T>C
  hgvsp: ENST00000419700.1:c.171T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.780T>C
  hgvsp: ENST00000376355.3:c.780T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.882T>C
  hgvsp: ENST00000339105.4:c.882T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.780T>C
  hgvsp: ENST00000444838.2:c.780T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.882T>C
  hgvsp: ENST00000376360.1:c.882T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.780T>C
  hgvsp: ENST00000376354.1:c.780T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7256
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4937
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5391
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6427
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7078
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1721
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1692
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2858
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8132
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2697
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala294Ala
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

13-100523280-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523280
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523280
    reference: chr 13
allele count: 1
allele frequency: 8.244702778464837e-6
allele num: 121290
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.789G>A
  hgvsp: ENST00000444838.2:c.789G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.180G>A
  hgvsp: ENST00000419700.1:c.180G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.891G>A
  hgvsp: ENST00000339105.4:c.891G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.891G>A
  hgvsp: ENST00000376360.1:c.891G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.9G>A
  hgvsp: ENST00000425186.2:c.9G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.789G>A
  hgvsp: ENST00000376355.3:c.789G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.789G>A
  hgvsp: ENST00000376354.1:c.789G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6000
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7080
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5409
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4938
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7254
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2857
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2683
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8186
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu297Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum

13-100523298-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523298
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523298
    reference: chr 13
allele count: 1
allele frequency: 8.242935804015958e-6
allele num: 121316
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.198A>T
  hgvsp: ENSP00000396574.1:p.Glu66Asp
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.807A>T
  hgvsp: ENSP00000365533.3:p.Glu269Asp
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.27A>T
  hgvsp: ENSP00000389062.1:p.Glu9Asp
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.909A>T
  hgvsp: ENSP00000342991.4:p.Glu303Asp
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.909A>T
  hgvsp: ENSP00000365538.1:p.Glu303Asp
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.807A>T
  hgvsp: ENSP00000404768.2:p.Glu269Asp
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.807A>T
  hgvsp: ENSP00000365532.1:p.Glu269Asp
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4586
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7076
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6306
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3503
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4937
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5427
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6422
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5994
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3141
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1718
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37578
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8209
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu303Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum

13-100523302-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523302
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523302
    reference: chr 13
allele count: 5
allele frequency: 4.121603798470061e-5
allele num: 121312
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.31C>T
  hgvsp: ENSP00000389062.1:p.Gln11Ter
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.811C>T
  hgvsp: ENSP00000365532.1:p.Gln271Ter
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.913C>T
  hgvsp: ENSP00000365538.1:p.Gln305Ter
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.811C>T
  hgvsp: ENSP00000404768.2:p.Gln271Ter
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.811C>T
  hgvsp: ENSP00000365533.3:p.Gln271Ter
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.202C>T
  hgvsp: ENSP00000396574.1:p.Gln68Ter
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.913C>T
  hgvsp: ENSP00000342991.4:p.Gln305Ter
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5421
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4585
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5991
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4936
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7073
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2855
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8193
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gln305Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

13-100523307-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523307
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523307
    reference: chr 13
allele count: 3
allele frequency: 2.472880741204788e-5
allele num: 121316
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.816A>G
  hgvsp: ENST00000376355.3:c.816A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.36A>G
  hgvsp: ENST00000425186.2:c.36A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.918A>G
  hgvsp: ENST00000339105.4:c.918A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.816A>G
  hgvsp: ENST00000376354.1:c.816A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.816A>G
  hgvsp: ENST00000444838.2:c.816A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.918A>G
  hgvsp: ENST00000376360.1:c.918A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.207A>G
  hgvsp: ENST00000419700.1:c.207A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7072
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3503
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7252
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5416
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6305
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5981
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4937
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2690
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8191
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gln306Gln
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

13-100523315-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523315
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523315
    reference: chr 13
allele count: 4
allele frequency: 3.297717979158422e-5
allele num: 121296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.824A>T
  hgvsp: ENSP00000404768.2:p.Lys275Met
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.215A>T
  hgvsp: ENSP00000396574.1:p.Lys72Met
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.824A>T
  hgvsp: ENSP00000365533.3:p.Lys275Met
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.926A>T
  hgvsp: ENSP00000342991.4:p.Lys309Met
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.926A>T
  hgvsp: ENSP00000365538.1:p.Lys309Met
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.44A>T
  hgvsp: ENSP00000389062.1:p.Lys15Met
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.824A>T
  hgvsp: ENSP00000365532.1:p.Lys275Met
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4594
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7252
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7071
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5384
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5972
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4938
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8166
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3120
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Lys309Met
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

13-100523321-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523321
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523321
    reference: chr 13
allele count: 2
allele frequency: 1.649130908011478e-5
allele num: 121276
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.216+5A>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.927+5A>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.825+5A>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.825+5A>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.45+5A>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.825+5A>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.927+5A>T
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6411
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5363
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4565
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7069
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5957
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4937
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1717
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2678
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3115
  bin: 6.75e1
  variant carriers: 0
hgvs: c.927+5A>T
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD

13-100523323-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523323
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523323
    reference: chr 13
allele count: 6
allele frequency: 4.9478007025877e-5
allele num: 121266
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.216+7G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.825+7G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.45+7G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.825+7G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.825+7G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.927+7G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.927+7G>A
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7069
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4938
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5362
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5957
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2363
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4556
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
hgvs: c.927+7G>A
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP

13-100523327-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523327
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523327
    reference: chr 13
allele count: 2
allele frequency: 1.649702228747711e-5
allele num: 121234
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.927+11T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.216+11T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.45+11T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.927+11T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.825+11T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.825+11T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.825+11T>C
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4543
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5919
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6405
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4938
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7067
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5309
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6305
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37570
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: T
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

13-100523339-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523339
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523339
    reference: chr 13
allele count: 1
allele frequency: 8.253549026081216e-6
allele num: 121160
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.825+23G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.825+23G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.927+23G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.45+23G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.825+23G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.927+23G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.216+23G>A
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7057
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7252
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5179
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5801
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4938
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7718
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2853
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff

13-100523340-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523340
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523340
    reference: chr 13
allele count: 2
allele frequency: 1.650628063978344e-5
allele num: 121166
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.927+24G>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.927+24G>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.216+24G>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.45+24G>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.825+24G>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.825+24G>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.825+24G>T
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6349
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4938
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6301
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7056
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5156
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2667
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7662
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1708
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2654
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

13-100523345-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523345
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523345
    reference: chr 13
allele count: 1216
allele frequency: 1.004062489678634e-2
allele num: 121108
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.927+29G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.45+29G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.216+29G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.825+29G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.825+29G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.927+29G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.825+29G>A
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5027
  bin: 2.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 7225
  bin: 4.75e1
  variant carriers: 93
genotype depth: GenotypeDepth
  all individuals: 2370
  bin: 6.75e1
  variant carriers: 95
genotype depth: GenotypeDepth
  all individuals: 3530
  bin: 6.25e1
  variant carriers: 111
genotype depth: GenotypeDepth
  all individuals: 6296
  bin: 5.25e1
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5695
  bin: 3.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 4920
  bin: 5.75e1
  variant carriers: 95
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 1.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 7029
  bin: 4.25e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 8.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 8.25e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 6292
  bin: 3.75e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 7.75e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 2614
  bin: 9.75e1
  variant carriers: 151
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 7.25e1
  variant carriers: 73
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2828
  bin: 9.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1625
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2629
  bin: 7.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 61
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum

13-100523348-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523348
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523348
    reference: chr 13
allele count: 1
allele frequency: 8.258865892535638e-6
allele num: 121082
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.216+32C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.825+32C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.825+32C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.45+32C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.825+32C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.927+32C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.927+32C>T
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5766
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7244
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3474
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4900
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6361
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4428
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1730
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37310
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2983
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum

13-100523362-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523362
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523362
    reference: chr 13
allele count: 0
allele frequency: 0.0e0
allele num: 120952
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.45+46T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.927+46T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.825+46T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.216+46T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.927+46T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.825+46T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.825+46T>C
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7089
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4900
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4526
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7240
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6295
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3474
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2662
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2759
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1589
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD

13-100523366-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523366
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523366
    reference: chr 13
allele count: 6
allele frequency: 4.96310756708467e-5
allele num: 120892
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.45+50C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.825+50C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.825+50C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.216+50C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.927+50C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.927+50C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.825+50C>T
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4505
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3475
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4900
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4952
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6280
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6317
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7235
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7093
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5371
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 786
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37295
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5572
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2880
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2672
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 758
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

13-100523367-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100523367
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100523367
    reference: chr 13
allele count: 3
allele frequency: 2.482498386376049e-5
allele num: 120846
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.216+51G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.45+51G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.927+51G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.927+51G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.825+51G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.825+51G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.825+51G>A
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3475
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7093
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4563
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7236
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4901
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1566
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 774
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2661
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1723
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2620
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

13-100529812-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100529812
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100529812
    reference: chr 13
allele count: 5
allele frequency: 1.872659176029963e-3
allele num: 2670
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.825+6496G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.825+6496G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.216+6496G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.927+6496G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.45+6496G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.927+6496G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.826-40G>A
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 723
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2679
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 840
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

13-100529812-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100529812
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100529812
    reference: chr 13
allele count: 0
allele frequency: 0.0e0
allele num: 2670
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.825+6496G>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.927+6496G>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.927+6496G>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.826-40G>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.45+6496G>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.216+6496G>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.825+6496G>T
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2679
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

13-100529819-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100529819
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100529819
    reference: chr 13
allele count: 5
allele frequency: 2.061005770816158e-3
allele num: 2426
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.825+6503G>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.927+6503G>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.826-33G>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.825+6503G>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.927+6503G>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.216+6503G>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.45+6503G>T
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 2044
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2782
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 747
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

13-100529822-A-ATTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100529822
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100529825
    reference: chr 13
allele count: 2
allele frequency: 4.434589800443459e-4
allele num: 4510
alternate allele: ATTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.45+6508_45+6509insTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.826-28_826-27insTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.927+6508_927+6509insTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.927+6508_927+6509insTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.825+6508_825+6509insTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.825+6508_825+6509insTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.216+6508_216+6509insTTT
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 785
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1625
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1125
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

13-100529822-ATTCT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100529822
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100529818
    reference: chr 13
allele count: 1
allele frequency: 2.217294900221729e-4
allele num: 4510
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.45+6509_45+6512delCTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.826-27_826-24delCTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.927+6509_927+6512delCTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.825+6509_825+6512delCTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.216+6509_216+6512delCTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.825+6509_825+6512delCTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.927+6509_927+6512delCTTT
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 785
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1625
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: ATTCT
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

13-100529825-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100529825
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100529826
    reference: chr 13
allele count: 4
allele frequency: 8.438818565400843e-3
allele num: 474
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.927+6532dupT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.216+6532dupT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.927+6532dupT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.45+6532dupT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.825+6532dupT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.825+6532dupT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.826-4dupT
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 2.5e0
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 7.5e0
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 1.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 1.25e1
  variant carriers: 34
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4319
  bin: 2.5e0
  variant carriers: 26
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 7.5e0
  variant carriers: 41
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD

13-100529825-C-CTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100529825
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100529827
    reference: chr 13
allele count: 4
allele frequency: 8.438818565400843e-3
allele num: 474
alternate allele: CTT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.927+6531_927+6532dupTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.927+6531_927+6532dupTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.45+6531_45+6532dupTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.825+6531_825+6532dupTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.826-5_826-4dupTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.825+6531_825+6532dupTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.216+6531_216+6532dupTT
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 7.5e0
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 2.5e0
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4319
  bin: 2.5e0
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 7.5e0
  variant carriers: 24
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 2
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

13-100529825-C-CTTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100529825
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100529828
    reference: chr 13
allele count: 6
allele frequency: 1.265822784810127e-2
allele num: 474
alternate allele: CTTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.826-6_826-4dupTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.825+6530_825+6532dupTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.927+6530_927+6532dupTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.216+6530_216+6532dupTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.45+6530_45+6532dupTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.927+6530_927+6532dupTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.825+6530_825+6532dupTTT
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 7.5e0
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 2.5e0
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 1.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 1.25e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 7.5e0
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4319
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.25e1
  variant carriers: 3
num of homozygotes: 2
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ

13-100529825-CTTTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100529825
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100529821
    reference: chr 13
allele count: 30
allele frequency: 6.329113924050633e-2
allele num: 474
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.927+6529_927+6532delTTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.825+6529_825+6532delTTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.45+6529_45+6532delTTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.216+6529_216+6532delTTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.927+6529_927+6532delTTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.826-7_826-4delTTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.825+6529_825+6532delTTTT
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 1.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 7.5e0
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4319
  bin: 2.5e0
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: CTTTT
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum

13-100529825-CTTTTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100529825
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100529820
    reference: chr 13
allele count: 17
allele frequency: 3.586497890295359e-2
allele num: 474
alternate allele: C
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 9.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4319
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 12
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 18
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 1
  allele frequency: 1.666666666666667e-1
  allele num: 6
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: NaN
  allele num: 0
  num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: CTTTTT
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD

13-100529825-C-CTTTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100529825
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100529829
    reference: chr 13
allele count: 1
allele frequency: 2.109704641350211e-3
allele num: 474
alternate allele: CTTTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.216+6529_216+6532dupTTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.927+6529_927+6532dupTTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.826-7_826-4dupTTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.45+6529_45+6532dupTTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.927+6529_927+6532dupTTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.825+6529_825+6532dupTTTT
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.825+6529_825+6532dupTTTT
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 7.5e0
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

13-100529857-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100529857
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100529857
    reference: chr 13
allele count: 1
allele frequency: 1.758705592683785e-4
allele num: 5686
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.825+6541G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.927+6541G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.825+6541G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.216+6541G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.927+6541G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.831G>A
  hgvsp: ENST00000444838.2:c.831G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.45+6541G>A
  variant of: http://identifiers.org/hgnc/18355
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3011
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val277Val
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

13-100529892-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100529892
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100529892
    reference: chr 13
allele count: 1
allele frequency: 1.918649270913277e-4
allele num: 5212
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.45+6576G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.927+6576G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.216+6576G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.825+6576G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.825+6576G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.866G>A
  hgvsp: ENSP00000404768.2:p.Arg289His
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.927+6576G>A
  variant of: http://identifiers.org/hgnc/18355
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3181
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
hgvs: p.Arg289His
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

13-100529899-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100529899
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100529899
    reference: chr 13
allele count: 2
allele frequency: 3.910833007430582e-4
allele num: 5114
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.927+6583C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.216+6583C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.873C>T
  hgvsp: ENST00000444838.2:c.873C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.825+6583C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.825+6583C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.927+6583C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.45+6583C>T
  variant of: http://identifiers.org/hgnc/18355
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2302
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3257
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1332
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu291Leu
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

13-100529916-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100529916
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100529916
    reference: chr 13
allele count: 1
allele frequency: 2.608242044861763e-4
allele num: 3834
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.825+6600C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.890C>T
  hgvsp: ENSP00000404768.2:p.Pro297Leu
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.216+6600C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.45+6600C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.927+6600C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.927+6600C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.825+6600C>T
  variant of: http://identifiers.org/hgnc/18355
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3293
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro297Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD

13-100529966-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100529966
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100529966
    reference: chr 13
allele count: 0
allele frequency: 0.0e0
allele num: 566
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.825+6650G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.*31G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.45+6650G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.927+6650G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.825+6650G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.216+6650G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.927+6650G>A
  variant of: http://identifiers.org/hgnc/18355
canonical: false
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3977
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1165
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 3789
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 448
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genotype quality: GenotypeQuality
  all individuals: 480
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genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

13-100529975-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100529975
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100529975
    reference: chr 13
allele count: 132
allele frequency: 2.907488986784141e-1
allele num: 454
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.45+6659C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.927+6659C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.216+6659C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.927+6659C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.825+6659C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000404768
  ensembl transcript: ENST00000444838
  gene symbol: CLYBL
  hgvsc: ENST00000444838.2:c.*40C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.825+6659C>T
  variant of: http://identifiers.org/hgnc/18355
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.25e1
  variant carriers: 116
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3432
  bin: 2.5e0
  variant carriers: 285
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 7.5e0
  variant carriers: 704
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 6.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 1217
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 8.75e1
  variant carriers: 53
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 8.25e1
  variant carriers: 95
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.25e1
  variant carriers: 28
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 1.25e1
  variant carriers: 92
genotype quality: GenotypeQuality
  all individuals: 613
  bin: 2.25e1
  variant carriers: 102
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.75e1
  variant carriers: 62
num of homozygotes: 10
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP

13-100537185-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100537185
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100537185
    reference: chr 13
allele count: 1
allele frequency: 5.87406015037594e-5
allele num: 17024
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.928-6387G>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.826-6387G>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.826-6387G>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.217-6387G>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.46-46G>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.928-6387G>C
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34933
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1885
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 631
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2182
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1597
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23366
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

13-100537193-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100537193
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100537193
    reference: chr 13
allele count: 0
allele frequency: 0.0e0
allele num: 17078
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.217-6379C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.46-38C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.826-6379C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.826-6379C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.928-6379C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.928-6379C>T
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35499
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 754
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5982
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27389
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2244
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

13-100537206-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100537206
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100537206
    reference: chr 13
allele count: 0
allele frequency: 0.0e0
allele num: 17406
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.928-6366A>G
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.826-6366A>G
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.217-6366A>G
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.928-6366A>G
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.826-6366A>G
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.46-25A>G
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35733
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3305
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7220
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3041
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 490
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5398
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1101
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31817
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/13-100537207-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100537207
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100537207
    reference: chr 13
allele count: 0
allele frequency: 0.0e0
allele num: 17418
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.46-24C>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.928-6365C>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.826-6365C>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.826-6365C>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.217-6365C>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.928-6365C>A
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7475
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35622
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2212
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31852
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3021
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5595
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 906
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS

13-100537208-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100537208
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100537208
    reference: chr 13
allele count: 29
allele frequency: 1.663416312951704e-3
allele num: 17434
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.928-6364C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.826-6364C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.928-6364C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.46-23C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.826-6364C>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.217-6364C>T
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7886
  bin: 7.5e0
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35406
  bin: 2.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3247
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2236
  bin: 9.75e1
  variant carriers: 31
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2364
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31822
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 2.75e1
  variant carriers: 4
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
reference allele: C
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

13-100537209-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100537209
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100537209
    reference: chr 13
allele count: 1
allele frequency: 5.684402000909504e-5
allele num: 17592
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.928-6363G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.826-6363G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.928-6363G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.826-6363G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.46-22G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.217-6363G>A
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8606
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1059
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1868
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32044
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2045
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6732
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3087
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

13-100537211-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100537211
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100537211
    reference: chr 13
allele count: 0
allele frequency: 0.0e0
allele num: 17676
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.928-6361A>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.826-6361A>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.46-20A>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.217-6361A>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.826-6361A>T
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.928-6361A>T
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34695
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9323
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1280
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7272
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1998
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1516
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 942
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3142
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31974
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum

13-100537214-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100537214
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100537214
    reference: chr 13
allele count: 0
allele frequency: 0.0e0
allele num: 17776
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.826-6358T>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.928-6358T>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.217-6358T>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.46-17T>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.928-6358T>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.826-6358T>A
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33972
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10364
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3379
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7993
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3146
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31612
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1594
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1272
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ

13-100537216-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100537216
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100537216
    reference: chr 13
allele count: 0
allele frequency: 0.0e0
allele num: 17862
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.217-6356T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.826-6356T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.928-6356T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.928-6356T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.826-6356T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.46-15T>C
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 11015
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33554
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8522
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1835
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1244
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1630
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2236
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 955
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS

13-100537217-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100537217
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100537217
    reference: chr 13
allele count: 0
allele frequency: 0.0e0
allele num: 17946
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.826-6355G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.928-6355G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.928-6355G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.826-6355G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.46-14G>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.217-6355G>A
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33346
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11323
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8821
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1711
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1799
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2234
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1027
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3206
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

13-100537221-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100537221
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100537221
    reference: chr 13
allele count: 18009
allele frequency: 7.569351042367182e-1
allele num: 23792
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.46-10T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.217-6351T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.826-6351T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.928-6351T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.826-6351T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.928-6351T>C
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.75e1
  variant carriers: 391
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 3.25e1
  variant carriers: 808
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 3.75e1
  variant carriers: 1054
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 4.75e1
  variant carriers: 813
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 175
genotype depth: GenotypeDepth
  all individuals: 20975
  bin: 7.5e0
  variant carriers: 18616
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 4.25e1
  variant carriers: 1013
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 9.75e1
  variant carriers: 1145
genotype depth: GenotypeDepth
  all individuals: 2985
  bin: 1.25e1
  variant carriers: 2915
genotype depth: GenotypeDepth
  all individuals: 17344
  bin: 2.5e0
  variant carriers: 13525
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 2.75e1
  variant carriers: 531
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 267
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 135
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 5.25e1
  variant carriers: 573
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 1.75e1
  variant carriers: 559
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 2.25e1
  variant carriers: 371
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 113
genotype quality: GenotypeQuality
  all individuals: 8655
  bin: 7.5e0
  variant carriers: 6776
genotype quality: GenotypeQuality
  all individuals: 5464
  bin: 2.25e1
  variant carriers: 5007
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 4.25e1
  variant carriers: 162
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 3.75e1
  variant carriers: 606
genotype quality: GenotypeQuality
  all individuals: 1787
  bin: 2.75e1
  variant carriers: 1778
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 8.75e1
  variant carriers: 334
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 7.25e1
  variant carriers: 150
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 5.25e1
  variant carriers: 346
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 9.25e1
  variant carriers: 594
genotype quality: GenotypeQuality
  all individuals: 1350
  bin: 6.25e1
  variant carriers: 748
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 5.75e1
  variant carriers: 579
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 6.75e1
  variant carriers: 419
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 4.75e1
  variant carriers: 288
num of homozygotes: 6927
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

13-100537222-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100537222
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100537222
    reference: chr 13
allele count: 0
allele frequency: 0.0e0
allele num: 23716
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.217-6350T>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.928-6350T>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.826-6350T>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.46-9T>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.826-6350T>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.928-6350T>A
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21924
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20605
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2903
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1369
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10069
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7741
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7093
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16657
  bin: 7.5e0
  variant carriers: 2
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

13-100537222-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100537222
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100537222
    reference: chr 13
allele count: 1
allele frequency: 4.2165626581211e-5
allele num: 23716
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.928-6350T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.826-6350T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.928-6350T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.46-9T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.217-6350T>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.826-6350T>C
  variant of: http://identifiers.org/hgnc/18355
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2903
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20605
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21924
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 820
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7741
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7093
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1455
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16657
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/13-100537223-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100537223
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100537223
    reference: chr 13
allele count: 0
allele frequency: 0.0e0
allele num: 23718
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.928-6349C>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.928-6349C>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.217-6349C>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.46-8C>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.826-6349C>A
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.826-6349C>A
  variant of: http://identifiers.org/hgnc/18355
canonical: false
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22114
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20624
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 560
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7615
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1462
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9554
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16867
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 560
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
hgvs: c.46-8C>A
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

13-100537231-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100537231
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 100537231
    reference: chr 13
allele count: 0
allele frequency: 0.0e0
allele num: 23866
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000396574
  ensembl transcript: ENST00000419700
  gene symbol: CLYBL
  hgvsc: ENST00000419700.1:c.217-6341G>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000342991
  ensembl transcript: ENST00000339105
  gene symbol: CLYBL
  hgvsc: ENST00000339105.4:c.928-6341G>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365538
  ensembl transcript: ENST00000376360
  gene symbol: CLYBL
  hgvsc: ENST00000376360.1:c.928-6341G>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365532
  ensembl transcript: ENST00000376354
  gene symbol: CLYBL
  hgvsc: ENST00000376354.1:c.826-6341G>C
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000389062
  ensembl transcript: ENST00000425186
  gene symbol: CLYBL
  hgvsc: ENST00000425186.2:c.46G>C
  hgvsp: ENSP00000389062.1:p.Val16Leu
  variant of: http://identifiers.org/hgnc/18355
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125246
  ensembl protein: ENSP00000365533
  ensembl transcript: ENST00000376355
  gene symbol: CLYBL
  hgvsc: ENST00000376355.3:c.826-6341G>C
  variant of: http://identifiers.org/hgnc/18355
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22415
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 9.75e1
  variant carriers: 0
hgvs: p.Val16Leu
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37601
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4048
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1416
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2418
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64592
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10198
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.598e0

DP
type: SiteQuality
SIO_000300: 2.864122e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.51e-1

QD
type: SiteQuality
SIO_000300: 2.483e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.51e-1

GenotypeQuality
all individuals: 40
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 676
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4123
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1412
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37601
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2810
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.698677800974252e-5
allele num: 11496
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64596
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.9e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

DP
type: SiteQuality
SIO_000300: 2.86535e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.143e1

MQRankSum
type: SiteQuality
SIO_000300: -9.91e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.932e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.75e0

GenotypeQuality
all individuals: 37606
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1677
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2367
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2406
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2530
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.192333890643384e-5
allele num: 64596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.782821365681862e-5
allele num: 10222
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.748e0

QD
type: SiteQuality
SIO_000300: 1.32e1

DP
type: SiteQuality
SIO_000300: 2.86767e6

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

FS
type: SiteQuality
SIO_000300: 1.679e0

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

GenotypeQuality
all individuals: 2566
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2810
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4207
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2532
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1414
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.093963676866434e-5
allele num: 64642
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.1e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.39e0

FS
type: SiteQuality
SIO_000300: 2.334e0

VQSLOD
type: SiteQuality
SIO_000300: 2.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.75e0

DP
type: SiteQuality
SIO_000300: 2.868404e6

QD
type: SiteQuality
SIO_000300: 1.34e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.94e-1

GenotypeQuality
all individuals: 2432
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 2530
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2872
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1676
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2405
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2809
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.730842971117571e-5
allele num: 64676
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.737098344693281e-5
allele num: 10270
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
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: 3
allele frequency: 2.609149417289963e-4
allele num: 11498
num of homozygotes: 0

South Asian
type: Population
allele count: 36
allele frequency: 3.466204506065858e-3
allele num: 10386
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.219e0

FS
type: SiteQuality
SIO_000300: 2.271e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

QD
type: SiteQuality
SIO_000300: 1.21e1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.0e0

DP
type: SiteQuality
SIO_000300: 2.87182e6

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2531
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1676
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2414
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2806
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2431
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.545499505440158e-5
allele num: 64704
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: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

Latino
type: Population
allele count: 11
allele frequency: 9.560229445506692e-4
allele num: 11506
num of homozygotes: 0

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

African
type: Population
allele count: 144
allele frequency: 1.401323472168159e-2
allele num: 10276
num of homozygotes: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10462
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.49e-1

QD
type: SiteQuality
SIO_000300: 1.261e1

FS
type: SiteQuality
SIO_000300: 6.5e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

MQRankSum
type: SiteQuality
SIO_000300: 1.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.85e0

DP
type: SiteQuality
SIO_000300: 2.874842e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.21e-1

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

GenotypeQuality
all individuals: 203
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3269
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2813
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2530
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.175507935527697e-5
allele num: 64772
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 4
allele frequency: 3.737619136609979e-4
allele num: 10702
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQ
type: SiteQuality
SIO_000300: 5.991e1

VQSLOD
type: SiteQuality
SIO_000300: 4.68e0

MQRankSum
type: SiteQuality
SIO_000300: 3.28e-1

DP
type: SiteQuality
SIO_000300: 2.875398e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.4e-1

QD
type: SiteQuality
SIO_000300: 1.298e1

GenotypeQuality
all individuals: 37571
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 4519
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2813
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 434
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 3.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.234263144902493e-4
allele num: 64816
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e-1

QD
type: SiteQuality
SIO_000300: 1.226e1

VQSLOD
type: SiteQuality
SIO_000300: 3.82e0

MQRankSum
type: SiteQuality
SIO_000300: 3.19e-1

DP
type: SiteQuality
SIO_000300: 2.876563e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.65e-1

GenotypeQuality
all individuals: 421
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1677
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1434
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2532
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2813
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 7.5e0
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10940
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.625204279855694e-5
allele num: 64862
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.878338e6

MQRankSum
type: SiteQuality
SIO_000300: 3.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e0

VQSLOD
type: SiteQuality
SIO_000300: 9.23e-1

QD
type: SiteQuality
SIO_000300: 1.043e1

MQ
type: SiteQuality
SIO_000300: 5.939e1

FS
type: SiteQuality
SIO_000300: 2.583e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

GenotypeQuality
all individuals: 4825
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1434
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37570
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1678
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2812
bin: 9.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.161710037174721e-4
allele num: 8608
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64912
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11182
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.706853038245001e-5
allele num: 10302
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

DP
type: SiteQuality
SIO_000300: 2.881814e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

QD
type: SiteQuality
SIO_000300: 1.042e1

MQ
type: SiteQuality
SIO_000300: 5.953e1

FS
type: SiteQuality
SIO_000300: 4.009e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.13e-1

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5070
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1677
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2812
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10314
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.075882009166129e-5
allele num: 65022
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.01e0

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

FS
type: SiteQuality
SIO_000300: 1.214e0

QD
type: SiteQuality
SIO_000300: 1.415e1

DP
type: SiteQuality
SIO_000300: 2.885883e6

GenotypeQuality
all individuals: 2487
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37571
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5118
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2812
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2425
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
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: 11522
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.537373551025428e-5
allele num: 65046
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10314
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.55e0

QD
type: SiteQuality
SIO_000300: 1.14e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.2e0

DP
type: SiteQuality
SIO_000300: 2.886616e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.89e-1

FS
type: SiteQuality
SIO_000300: 6.830000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.725e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

GenotypeQuality
all individuals: 2559
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2464
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1479
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2813
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1679
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521931026085898e-5
allele num: 65706
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13526
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.962e0

MQRankSum
type: SiteQuality
SIO_000300: -1.336e0

DP
type: SiteQuality
SIO_000300: 2.91077e6

FS
type: SiteQuality
SIO_000300: 9.05e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.53e-2

QD
type: SiteQuality
SIO_000300: 1.18e1

VQSLOD
type: SiteQuality
SIO_000300: -6.69e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e-1

GenotypeQuality
all individuals: 1657
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2701
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6687
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37570
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2478
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1510
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14136
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517727051966974e-5
allele num: 65888
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.68e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.81e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.64e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.18e-1

DP
type: SiteQuality
SIO_000300: 2.919269e6

VQSLOD
type: SiteQuality
SIO_000300: -8.326e-1

QD
type: SiteQuality
SIO_000300: 1.115e1

GenotypeQuality
all individuals: 203
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2820
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37574
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 89
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1691
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2591
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1529
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6770
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14374
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.643201542912247e-5
allele num: 10370
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65998
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -7.533e-1

DP
type: SiteQuality
SIO_000300: 2.922735e6

FS
type: SiteQuality
SIO_000300: 1.448e0

MQRankSum
type: SiteQuality
SIO_000300: -1.723e0

MQ
type: SiteQuality
SIO_000300: 5.892e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.19e0

QD
type: SiteQuality
SIO_000300: 1.217e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.1e-1

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37582
bin: 9.75e1
variant carriers: 25

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2868
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variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2623
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.034092623321768e-5
allele num: 66290
num of homozygotes: 0

African
type: Population
allele count: 12
allele frequency: 1.155401502021953e-3
allele num: 10386
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.191209551825575e-4
allele num: 11558
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: 898
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.949064449064449e-4
allele num: 15392
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.88e0

QD
type: SiteQuality
SIO_000300: 1.315e1

VQSLOD
type: SiteQuality
SIO_000300: 6.09e0

DP
type: SiteQuality
SIO_000300: 2.937803e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

GenotypeQuality
all individuals: 2629
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 62
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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: 1713
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variant carriers: 0

GenotypeQuality
all individuals: 37578
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
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: 8646
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15928
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505162708088744e-5
allele num: 66438
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.947e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.48e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.318e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.56e-2

FS
type: SiteQuality
SIO_000300: 7.04e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.944966e6

QD
type: SiteQuality
SIO_000300: 1.106e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.237e0

GenotypeQuality
all individuals: 59
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2661
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 63
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variant carriers: 0

GenotypeQuality
all individuals: 2650
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variant carriers: 0

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

GenotypeQuality
all individuals: 47
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16218
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
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: 6602
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.968e1

DP
type: SiteQuality
SIO_000300: 2.950572e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.36e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.82e-1

QD
type: SiteQuality
SIO_000300: 1.648e1

FS
type: SiteQuality
SIO_000300: 5.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.32e0

GenotypeQuality
all individuals: 43
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
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variant carriers: 0

GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 1723
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variant carriers: 0

GenotypeQuality
all individuals: 50
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 23
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GenotypeQuality
all individuals: 2843
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 2.884615384615385e-4
allele num: 10400
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16248
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.005349522149426e-5
allele num: 66548
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: 11566
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.04e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.92e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.187e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.97e-1

QD
type: SiteQuality
SIO_000300: 1.2e1

FS
type: SiteQuality
SIO_000300: 3.269e0

MQRankSum
type: SiteQuality
SIO_000300: -5.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.76e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

DP
type: SiteQuality
SIO_000300: 2.951541e6

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

GenotypeQuality
all individuals: 7979
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 40
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variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 1692
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variant carriers: 0

GenotypeQuality
all individuals: 37581
bin: 9.75e1
variant carriers: 1

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502087902184036e-5
allele num: 66574
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16374
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -2.33e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.3e-1

QD
type: SiteQuality
SIO_000300: 1.381e1

VQSLOD
type: SiteQuality
SIO_000300: 7.28e-1

FS
type: SiteQuality
SIO_000300: 1.769e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.944e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.21e-2

DP
type: SiteQuality
SIO_000300: 2.953987e6

GenotypeQuality
all individuals: 1693
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2850
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 37581
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 33
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variant carriers: 0

GenotypeQuality
all individuals: 2683
bin: 8.25e1
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GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66584
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.101281269066504e-5
allele num: 16390
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.95e-1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -6.4e-2

DP
type: SiteQuality
SIO_000300: 2.954278e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.23e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.29e-1

FS
type: SiteQuality
SIO_000300: 1.8902e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.529999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.047e0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 8013
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16400
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.003544182134919e-5
allele num: 66588
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.782e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.13e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.57e0

MQ
type: SiteQuality
SIO_000300: 6.03e1

DP
type: SiteQuality
SIO_000300: 2.954704e6

BaseQRankSum
type: SiteQuality
SIO_000300: 8.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.16e-1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.123e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3101
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variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16416
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66604
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.747e1

VQSLOD
type: SiteQuality
SIO_000300: 2.41e-1

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.38e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.69e-1

FS
type: SiteQuality
SIO_000300: 3.283e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.47e0

DP
type: SiteQuality
SIO_000300: 2.955048e6

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 1721
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GenotypeQuality
all individuals: 20
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GenotypeQuality
all individuals: 25
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GenotypeQuality
all individuals: 3111
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GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 2852
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GenotypeQuality
all individuals: 2692
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.082725060827251e-5
allele num: 16440
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66624
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -9.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

DP
type: SiteQuality
SIO_000300: 2.955584e6

VQSLOD
type: SiteQuality
SIO_000300: 4.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.27e0

FS
type: SiteQuality
SIO_000300: 1.571e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.161e0

QD
type: SiteQuality
SIO_000300: 1.243e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.38e-2

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66630
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 2.956486e6

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.359e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.54e-2

FS
type: SiteQuality
SIO_000300: 1.3122e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.699e0

VQSLOD
type: SiteQuality
SIO_000300: -3.108e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.39e0

MQ
type: SiteQuality
SIO_000300: 5.986e1

QD
type: SiteQuality
SIO_000300: 1.561e1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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: 2

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

South Asian
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allele count: 1
allele frequency: 6.070908207867897e-5
allele num: 16472
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: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500645277469312e-5
allele num: 66638
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.83e0

FS
type: SiteQuality
SIO_000300: 3.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.9e-2

DP
type: SiteQuality
SIO_000300: 2.956751e6

MQRankSum
type: SiteQuality
SIO_000300: -2.62e-1

QD
type: SiteQuality
SIO_000300: 1.252e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.58e-2

MQ
type: SiteQuality
SIO_000300: 5.965e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500105007350515e-5
allele num: 66662
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.29e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.47e-1

DP
type: SiteQuality
SIO_000300: 2.957201e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.041e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.037e0

QD
type: SiteQuality
SIO_000300: 9.94e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e-1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 2697
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66674
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.69e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.56e-1

MQ
type: SiteQuality
SIO_000300: 5.909e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

QD
type: SiteQuality
SIO_000300: 1.091e1

FS
type: SiteQuality
SIO_000300: 1.204e0

DP
type: SiteQuality
SIO_000300: 2.957112e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.74e-1

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37577
bin: 9.75e1
variant carriers: 5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 1718
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.499175090740018e-5
allele num: 66674
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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: 6610
num of homozygotes: 0

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

Latino
type: Population
allele count: 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: 16502
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.956913e6

MQ
type: SiteQuality
SIO_000300: 5.971e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -3.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.19e-1

QD
type: SiteQuality
SIO_000300: 1.337e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.145e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.75e-1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 1690
bin: 7.25e1
variant carriers: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999490086685263e-5
allele num: 66678
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.978e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.164e1

DP
type: SiteQuality
SIO_000300: 2.956574e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

MQRankSum
type: SiteQuality
SIO_000300: -4.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.2e-2

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66668
num of homozygotes: 0

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

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

African
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allele count: 4
allele frequency: 3.851338340073175e-4
allele num: 10386
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
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

DP
type: SiteQuality
SIO_000300: 2.95589e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 6.15e-1

FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.958e1

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -4.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.519e0

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.422e1

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

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

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.00048007681229e-5
allele num: 66656
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.95471e6

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.744e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e-1

QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

South Asian
type: Population
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allele frequency: 3.636363636363636e-4
allele num: 16500
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.216e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 8.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.3e-1

QD
type: SiteQuality
SIO_000300: 1.005e1

DP
type: SiteQuality
SIO_000300: 2.954783e6

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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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2855
bin: 9.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66628
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.212121212121212e-4
allele num: 16500
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.169e1

FS
type: SiteQuality
SIO_000300: 7.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.85e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

DP
type: SiteQuality
SIO_000300: 2.952886e6

GenotypeQuality
all individuals: 163
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2656
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1661
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3028
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501862309263487e-5
allele num: 66584
num of homozygotes: 0

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.05e-1

FS
type: SiteQuality
SIO_000300: 2.3e0

VQSLOD
type: SiteQuality
SIO_000300: 2.89e-1

DP
type: SiteQuality
SIO_000300: 2.94688e6

MQRankSum
type: SiteQuality
SIO_000300: 5.3e-2

QD
type: SiteQuality
SIO_000300: 1.04e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.419e0

MQ
type: SiteQuality
SIO_000300: 5.905e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

GenotypeQuality
all individuals: 37
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2854
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 37558
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3024
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.935359009096187e-4
allele num: 10334
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66590
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.0971e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.360000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

VQSLOD
type: SiteQuality
SIO_000300: -1.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.029e0

QD
type: SiteQuality
SIO_000300: 1.486e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.04e-1

DP
type: SiteQuality
SIO_000300: 2.946193e6

GenotypeQuality
all individuals: 24
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37789
bin: 9.75e1
variant carriers: 1143

GenotypeQuality
all individuals: 85
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 150
bin: 2.75e1
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: 2

GenotypeQuality
all individuals: 1693
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 59
allele frequency: 5.097632624848799e-3
allele num: 11574
num of homozygotes: 0

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

Other
type: Population
allele count: 5
allele frequency: 5.518763796909493e-3
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 39
allele frequency: 2.363922899745424e-3
allele num: 16498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 23
allele frequency: 3.455321194639745e-4
allele num: 66564
num of homozygotes: 0

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

African
type: Population
allele count: 1090
allele frequency: 1.057841614906832e-1
allele num: 10304
num of homozygotes: 61

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.34e-2

DP
type: SiteQuality
SIO_000300: 2.948972e6

QD
type: SiteQuality
SIO_000300: 1.36e1

MQ
type: SiteQuality
SIO_000300: 5.969e1

MQRankSum
type: SiteQuality
SIO_000300: 2.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.97e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.72e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.88e-1

FS
type: SiteQuality
SIO_000300: 1.354e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.819e0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2674
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1650
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 358
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2883
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variant carriers: 0

GenotypeQuality
all individuals: 2684
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variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.062075654704171e-5
allele num: 16496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10290
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

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: 11570
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.75e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.927382e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.918e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.98e-1

QD
type: SiteQuality
SIO_000300: 1.073e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.39e-1

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

GenotypeQuality
all individuals: 49
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variant carriers: 0

GenotypeQuality
all individuals: 346
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variant carriers: 0

GenotypeQuality
all individuals: 6368
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 341
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variant carriers: 0

GenotypeQuality
all individuals: 1726
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variant carriers: 0

GenotypeQuality
all individuals: 2645
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variant carriers: 0

GenotypeQuality
all individuals: 366
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variant carriers: 0

GenotypeQuality
all individuals: 2879
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variant carriers: 0

GenotypeQuality
all individuals: 37301
bin: 9.75e1
variant carriers: 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: 906
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10234
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66504
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.04e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 2.917019e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 8.619999999999999e0

GenotypeQuality
all individuals: 387
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 41
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variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2612
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1564
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.313208420078649e-4
allele num: 8646
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.513178481165002e-5
allele num: 66472
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 9.9e0

FS
type: SiteQuality
SIO_000300: 2.679e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.69e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.92e0

DP
type: SiteQuality
SIO_000300: 2.915314e6

GenotypeQuality
all individuals: 895
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 44
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GenotypeQuality
all individuals: 504
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variant carriers: 0

GenotypeQuality
all individuals: 2877
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 5318
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.658008658008658e-5
allele num: 11550
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10208
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.00960062599693e-5
allele num: 66454
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.878e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.53e-1

MQ
type: SiteQuality
SIO_000300: 5.898e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.63e-1

DP
type: SiteQuality
SIO_000300: 2.914975e6

VQSLOD
type: SiteQuality
SIO_000300: -9.903999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.21e-1

QD
type: SiteQuality
SIO_000300: 1.168e1

GenotypeQuality
all individuals: 5
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 134
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variant carriers: 0

GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 2

GenotypeQuality
all individuals: 268
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 1

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.492537313432836e-3
allele num: 670
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.19047619047619e-2
allele num: 84
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.664816870144284e-3
allele num: 1802
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.83e-2

QD
type: SiteQuality
SIO_000300: 4.39e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.917e0

MQRankSum
type: SiteQuality
SIO_000300: -2.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.56e-1

FS
type: SiteQuality
SIO_000300: 1.931e2

DP
type: SiteQuality
SIO_000300: 7.3745e4

VQSLOD
type: SiteQuality
SIO_000300: -1.716e2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.15e-1

MQ
type: SiteQuality
SIO_000300: 5.357e1

GenotypeQuality
all individuals: 840
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 723
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 8.25e1
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GenotypeQuality
all individuals: 372
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 84
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 670
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1802
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.83e-2

FS
type: SiteQuality
SIO_000300: 1.931e2

QD
type: SiteQuality
SIO_000300: 4.39e0

VQSLOD
type: SiteQuality
SIO_000300: -1.716e2

ClippingRankSum
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SIO_000300: 4.56e-1

ReadPosRankSum
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SIO_000300: -3.15e-1

MQ
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SIO_000300: 5.357e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.917e0

DP
type: SiteQuality
SIO_000300: 7.3745e4

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: NaN
allele num: 0
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Other
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European (Non-Finnish)
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allele frequency: 1.65016501650165e-3
allele num: 606
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Latino
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South Asian
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allele frequency: 1.833740831295844e-3
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East Asian
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allele frequency: 1.666666666666667e-2
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
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MQ
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DP
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VQSLOD
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FS
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BaseQRankSum
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ClippingRankSum
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SIO_000300: 5.72e-1

QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: NaN
allele num: 0
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European (Non-Finnish)
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allele frequency: 1.801801801801802e-3
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Latino
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East Asian
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South Asian
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allele frequency: 0.0e0
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African
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Other
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InbreedingCoeff
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SIO_000300: 1.541e-1

FS
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BaseQRankSum
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MQRankSum
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VQSLOD
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QD
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DP
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ReadPosRankSum
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SIO_000300: -5.5e-1

MQ
type: SiteQuality
SIO_000300: 5.543e1

ClippingRankSum
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SIO_000300: 3.22e-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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East Asian
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allele frequency: 1.111111111111111e-2
allele num: 90
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 1110
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South Asian
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allele frequency: 0.0e0
allele num: 3112
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

FS
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SIO_000300: 8.2657e1

MQRankSum
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QD
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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SIO_000300: 1.541e-1

DP
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SIO_000300: 7.7052e4

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-1

MQ
type: SiteQuality
SIO_000300: 5.543e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 8.928571428571428e-3
allele num: 112
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East Asian
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African
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South Asian
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allele frequency: 0.0e0
allele num: 324
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European (Finnish)
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allele frequency: NaN
allele num: 0
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Latino
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allele frequency: 1.666666666666667e-1
allele num: 6
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.419e1

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.620000000000001e-1

DP
type: SiteQuality
SIO_000300: 7.2466e4

ReadPosRankSum
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QD
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InbreedingCoeff
type: SiteQuality
SIO_000300: 6.246e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.08e0

GenotypeQuality
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variant carriers: 14

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 6
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African
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allele frequency: 0.0e0
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Other
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East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.172839506172839e-3
allele num: 324
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European (Non-Finnish)
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allele frequency: 1.785714285714286e-2
allele num: 112
num of homozygotes: 1

DP
type: SiteQuality
SIO_000300: 7.2466e4

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.620000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.419e1

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 2
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 1.785714285714286e-2
allele num: 112
num of homozygotes: 0

East Asian
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allele frequency: 1.666666666666667e-1
allele num: 12
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South Asian
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allele frequency: 6.172839506172839e-3
allele num: 324
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ReadPosRankSum
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VQSLOD
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
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MQRankSum
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FS
type: SiteQuality
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QD
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MQ
type: SiteQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 5.555555555555555e-2
allele num: 324
num of homozygotes: 0

European (Non-Finnish)
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allele num: 112
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East Asian
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Other
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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African
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allele frequency: 1.111111111111111e-1
allele num: 18
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MQRankSum
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MQ
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ClippingRankSum
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FS
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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DP
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QD
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ReadPosRankSum
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European (Non-Finnish)
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South Asian
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Other
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FS
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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DP
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ReadPosRankSum
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BaseQRankSum
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MQ
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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East Asian
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 8.928571428571428e-3
allele num: 112
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Latino
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Other
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FS
type: SiteQuality
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BaseQRankSum
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MQ
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InbreedingCoeff
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QD
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VQSLOD
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MQRankSum
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ReadPosRankSum
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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African
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Latino
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European (Non-Finnish)
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European (Finnish)
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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FS
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MQRankSum
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MQ
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BaseQRankSum
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DP
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 480
bin: 6.25e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1360
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 2.844141069397042e-4
allele num: 3516
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 108
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.67e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.348e0

MQRankSum
type: SiteQuality
SIO_000300: 5.72e-1

FS
type: SiteQuality
SIO_000300: 2.963e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-2

DP
type: SiteQuality
SIO_000300: 6.3779e4

MQ
type: SiteQuality
SIO_000300: 5.742e1

QD
type: SiteQuality
SIO_000300: 6.34e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e-1

GenotypeQuality
all individuals: 458
bin: 6.25e1
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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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Other
type: Population
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allele frequency: 0.0e0
allele num: 48
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1350
num of homozygotes: 0

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

South Asian
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allele count: 2
allele frequency: 5.827505827505828e-4
allele num: 3432
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 114
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.503e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.45e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.531e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.65e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.618e0

QD
type: SiteQuality
SIO_000300: 3.9e0

FS
type: SiteQuality
SIO_000300: 1.596e0

DP
type: SiteQuality
SIO_000300: 6.2666e4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.65e-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: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1040
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 96
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 98
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 3.952569169960474e-4
allele num: 2530
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.226e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.5e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.52e-1

MQ
type: SiteQuality
SIO_000300: 4.795e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.65e0

QD
type: SiteQuality
SIO_000300: 7.37e0

FS
type: SiteQuality
SIO_000300: 2.363e0

DP
type: SiteQuality
SIO_000300: 5.2441e4

VQSLOD
type: SiteQuality
SIO_000300: -2.215e0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 290
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.960000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.09e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

MQ
type: SiteQuality
SIO_000300: 5.445e1

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.298e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.9728e4

GenotypeQuality
all individuals: 41
bin: 2.75e1
variant carriers: 21

GenotypeQuality
all individuals: 2679
bin: 7.5e0
variant carriers: 117

GenotypeQuality
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bin: 5.25e1
variant carriers: 71

GenotypeQuality
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bin: 1.75e1
variant carriers: 132

GenotypeQuality
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bin: 5.75e1
variant carriers: 27

GenotypeQuality
all individuals: 14
bin: 9.25e1
variant carriers: 14

GenotypeQuality
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variant carriers: 156

GenotypeQuality
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variant carriers: 15

GenotypeQuality
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variant carriers: 14

GenotypeQuality
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bin: 7.75e1
variant carriers: 65

European (Non-Finnish)
type: Population
allele count: 40
allele frequency: 2.469135802469136e-1
allele num: 162
num of homozygotes: 1

African
type: Population
allele count: 3
allele frequency: 1.666666666666667e-1
allele num: 18
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.666666666666667e-1
allele num: 6
num of homozygotes: 0

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

South Asian
type: Population
allele count: 66
allele frequency: 3.027522935779817e-1
allele num: 218
num of homozygotes: 4

East Asian
type: Population
allele count: 22
allele frequency: 4.782608695652174e-1
allele num: 46
num of homozygotes: 5

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.47e-2

FS
type: SiteQuality
SIO_000300: 1.188e0

VQSLOD
type: SiteQuality
SIO_000300: 2.62e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 1.76e1

MQ
type: SiteQuality
SIO_000300: 5.521e1

DP
type: SiteQuality
SIO_000300: 2.9219e4

GenotypeQuality
all individuals: 9192
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3247
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 612
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variant carriers: 0

GenotypeQuality
all individuals: 347
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 303
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5916
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1022
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 330
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.361655773420479e-4
allele num: 7344
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1688
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.08e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.728e0

DP
type: SiteQuality
SIO_000300: 4.19126e5

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.514e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.47e-1

MQ
type: SiteQuality
SIO_000300: 5.855e1

MQRankSum
type: SiteQuality
SIO_000300: -3.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.89e-1

QD
type: SiteQuality
SIO_000300: 1.028e1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2463
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 136
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3032
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1694
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7356
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 328
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1030
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 218
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5938
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.630000000000001e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.679999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.27e-1

QD
type: SiteQuality
SIO_000300: 2.113e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.129e0

VQSLOD
type: SiteQuality
SIO_000300: -1.26e-1

DP
type: SiteQuality
SIO_000300: 4.34899e5

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
all individuals: 349
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variant carriers: 0

GenotypeQuality
all individuals: 2250
bin: 1.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6094
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7472
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 532
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 334
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1702
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.99e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 4.70456e5

QD
type: SiteQuality
SIO_000300: 1.367e1

GenotypeQuality
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bin: 2.5e0
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
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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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 334
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6110
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1700
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 532
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 1052
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.96e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 6.21e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 8.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

DP
type: SiteQuality
SIO_000300: 4.72867e5

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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bin: 1.25e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 2

South Asian
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allele count: 24
allele frequency: 3.209414281893554e-3
allele num: 7478
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 222
num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 8.164598301763554e-4
allele num: 6124
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
allele num: 530
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 334
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.77247e5

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 2.4e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.887e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.84e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-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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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 1060
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 222
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 340
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6208
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 530
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1706
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.328727079457879e-4
allele num: 7526
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.79e-2

QD
type: SiteQuality
SIO_000300: 3.312e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

DP
type: SiteQuality
SIO_000300: 4.83607e5

ClippingRankSum
type: SiteQuality
SIO_000300: -7.29e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.504e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.04e-1

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

GenotypeQuality
all individuals: 38
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 532
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2232
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1064
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1714
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6250
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7550
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 346
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.65e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

QD
type: SiteQuality
SIO_000300: 1.335e1

DP
type: SiteQuality
SIO_000300: 4.89494e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

GenotypeQuality
all individuals: 416
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1886
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 547
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2233
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 224
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 348
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1720
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 536
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7582
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6298
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1068
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.419999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.57e0

DP
type: SiteQuality
SIO_000300: 4.97662e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 224
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3195
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31376
bin: 7.5e0
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 224
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6334
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1730
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1078
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 348
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 538
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7610
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.275e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 5.03019e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

QD
type: SiteQuality
SIO_000300: 3.011e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.96e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31323
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 962
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 9.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 224
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6388
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 352
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1742
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1088
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7610
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.05445e5

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.923e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.22e-2

VQSLOD
type: SiteQuality
SIO_000300: 9.63e-1

GenotypeQuality
all individuals: 4091
bin: 2.5e0
variant carriers: 338

GenotypeQuality
all individuals: 1382
bin: 3.25e1
variant carriers: 1371

GenotypeQuality
all individuals: 159
bin: 7.75e1
variant carriers: 142

GenotypeQuality
all individuals: 9167
bin: 9.75e1
variant carriers: 9138

GenotypeQuality
all individuals: 5569
bin: 1.25e1
variant carriers: 5487

GenotypeQuality
all individuals: 8816
bin: 1.75e1
variant carriers: 8759

GenotypeQuality
all individuals: 262
bin: 8.25e1
variant carriers: 249

Other
type: Population
allele count: 201
allele frequency: 7.8515625e-1
allele num: 256
num of homozygotes: 82

European (Finnish)
type: Population
allele count: 1853
allele frequency: 8.399818676337262e-1
allele num: 2206
num of homozygotes: 775

South Asian
type: Population
allele count: 4827
allele frequency: 6.119421906693712e-1
allele num: 7888
num of homozygotes: 1507

East Asian
type: Population
allele count: 733
allele frequency: 8.254504504504504e-1
allele num: 888
num of homozygotes: 294

Latino
type: Population
allele count: 549
allele frequency: 8.742038216560509e-1
allele num: 628
num of homozygotes: 244

African
type: Population
allele count: 1644
allele frequency: 9.309173272933182e-1
allele num: 1766
num of homozygotes: 762

European (Non-Finnish)
type: Population
allele count: 8202
allele frequency: 8.072834645669291e-1
allele num: 10160
num of homozygotes: 3263

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.357e0

VQSLOD
type: SiteQuality
SIO_000300: 1.054e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.521e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

QD
type: SiteQuality
SIO_000300: 2.897e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 7.47519e5

GenotypeQuality
all individuals: 292
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1455
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5939
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 820
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1774
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10138
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2210
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 250
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7870
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.54e-1

QD
type: SiteQuality
SIO_000300: 1.471e1

FS
type: SiteQuality
SIO_000300: 3.522e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.13e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.68e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.22e-1

DP
type: SiteQuality
SIO_000300: 7.46253e5

GenotypeQuality
all individuals: 186
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1369
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10069
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5939
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 119
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.270648030495553e-4
allele num: 7870
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1774
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2210
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10138
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 250
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.46253e5

FS
type: SiteQuality
SIO_000300: 3.522e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.13e-2

QD
type: SiteQuality
SIO_000300: 1.471e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.68e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.54e-1

GenotypeQuality
all individuals: 1368
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5938
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2212
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1774
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10142
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 250
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 612
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.11e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

DP
type: SiteQuality
SIO_000300: 7.4742e5

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.51e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.299e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.42e-1