17-37785845-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37785845
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37785845
    reference: chr 17
allele count: 18
allele frequency: 1.513520785685457e-4
allele num: 118928
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.265+30G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.57+30G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.57+30G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+30G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.165+30G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.189+30G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.165+30G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.156+30G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+362G>A
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2918
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12810
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2982
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6710
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8452
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17579
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1116
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1179
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21756
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum

17-37785847-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37785847
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37785847
    reference: chr 17
allele count: 565
allele frequency: 4.752531879815619e-3
allele num: 118884
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+364T>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+32T>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.189+32T>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.265+32T>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.57+32T>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.156+32T>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.57+32T>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.165+32T>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.165+32T>A
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.25e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6689
  bin: 3.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 1.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 12707
  bin: 3.25e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 5.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 17315
  bin: 2.75e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8247
  bin: 2.25e1
  variant carriers: 75
genotype depth: GenotypeDepth
  all individuals: 3411
  bin: 1.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 4.75e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 4.25e1
  variant carriers: 68
genotype quality: GenotypeQuality
  all individuals: 1286
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8647
  bin: 6.75e1
  variant carriers: 1
num of homozygotes: 11
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff

17-37785849-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37785849
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37785849
    reference: chr 17
allele count: 5
allele frequency: 4.211590296495957e-5
allele num: 118720
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+34C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.57+34C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.57+34C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.189+34C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+366C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.165+34C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.165+34C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.265+34C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.156+34C>T
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16858
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7908
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12626
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6693
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4256
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1928
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6650
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 716
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3417
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

17-37785853-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37785853
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37785853
    reference: chr 17
allele count: 6
allele frequency: 5.056549073808761e-5
allele num: 118658
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+370G>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+38G>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.57+38G>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.156+38G>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.165+38G>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.265+38G>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.165+38G>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.189+38G>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.57+38G>C
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5854
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15801
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6634
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12165
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7785
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1532
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2152
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6649
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1028
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2518
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/17-37785855-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37785855
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37785855
    reference: chr 17
allele count: 1
allele frequency: 8.437252155717926e-6
allele num: 118522
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+40C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.165+40C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.57+40C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.265+40C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.57+40C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.165+40C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+372C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.156+40C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.189+40C>A
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5840
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7881
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15814
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3426
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12072
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6615
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3254
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2236
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7856
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1446
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2546
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

17-37785856-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37785856
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37785856
    reference: chr 17
allele count: 1
allele frequency: 8.432698632216282e-6
allele num: 118586
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.57+41C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+373C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.165+41C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.165+41C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.189+41C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+41C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.156+41C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.265+41C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.57+41C>T
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15632
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11992
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3424
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7931
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6603
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6047
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1259
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1462
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4396
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7835
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum

17-37785862-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37785862
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37785862
    reference: chr 17
allele count: 178
allele frequency: 1.504852727334212e-3
allele num: 118284
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.265+47G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.189+47G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+47G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.156+47G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.165+47G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.57+47G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+379G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.165+47G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.57+47G>A
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9953
  bin: 2.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6536
  bin: 3.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 11287
  bin: 3.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 13748
  bin: 2.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 4.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6595
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 4.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 3110
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1778
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2125
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 7.5e0
  variant carriers: 1
num of homozygotes: 1
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

17-37786152-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37786152
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37786152
    reference: chr 17
allele count: 1
allele frequency: 9.000576036866359e-6
allele num: 111104
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.166-73T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.166-73T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.266-73T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.58-73T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+337T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.190-73T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.157-73T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.58-73T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+669T>C
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3843
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2591
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14546
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9586
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10338
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5285
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10830
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12178
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2746
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5122
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2857
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4402
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

17-37786162-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37786162
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37786162
    reference: chr 17
allele count: 1
allele frequency: 8.867292106336567e-6
allele num: 112774
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.266-63T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.157-63T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.166-63T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.58-63T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+679T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.166-63T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+347T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.190-63T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.58-63T>C
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2621
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20271
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3727
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10759
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8802
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5301
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1503
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3536
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2638
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

17-37786172-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37786172
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37786172
    reference: chr 17
allele count: 2
allele frequency: 1.754293633668404e-5
allele num: 114006
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.166-53G>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.190-53G>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.157-53G>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.166-53G>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+357G>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+689G>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.58-53G>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.266-53G>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.58-53G>C
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6334
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5876
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2541
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6806
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3518
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 726
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

17-37786174-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37786174
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37786174
    reference: chr 17
allele count: 1
allele frequency: 8.738814317673378e-6
allele num: 114432
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.266-51G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.157-51G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+359G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.58-51G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.166-51G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.166-51G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.58-51G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+691G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.190-51G>A
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2695
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5159
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25102
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1697
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3739
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6992
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4119
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum

17-37786190-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37786190
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37786190
    reference: chr 17
allele count: 1
allele frequency: 8.436825053995681e-6
allele num: 118528
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.58-35G>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.266-35G>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.58-35G>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.190-35G>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.166-35G>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.166-35G>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.157-35G>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+707G>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+375G>C
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29680
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14687
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8005
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3303
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

17-37786193-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37786193
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37786193
    reference: chr 17
allele count: 1
allele frequency: 8.392218734789103e-6
allele num: 119158
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.157-32G>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.166-32G>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.58-32G>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.190-32G>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+710G>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.266-32G>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.58-32G>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.166-32G>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+378G>T
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2865
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29988
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14959
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7565
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8119
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1463
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

17-37786205-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37786205
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37786205
    reference: chr 17
allele count: 4
allele frequency: 3.323473694705706e-5
allele num: 120356
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.166-20C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.266-20C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.190-20C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+722C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+390C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.58-20C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.58-20C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.157-20C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.166-20C>T
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7752
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15538
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2911
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34030
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1261
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

17-37786214-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37786214
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37786213
    reference: chr 17
allele count: 2
allele frequency: 1.657742486282181e-5
allele num: 120646
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.157-7delC
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.58-7delC
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.58-7delC
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.190-7delC
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.166-7delC
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.266-7delC
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+735delC
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.166-7delC
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+403delC
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2894
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15745
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30459
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8388
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4176
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: TC
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/17-37786215-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37786215
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37786215
    reference: chr 17
allele count: 2
allele frequency: 1.657412778652524e-5
allele num: 120670
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.58-10C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.166-10C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+732C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.190-10C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+400C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.157-10C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.58-10C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.266-10C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.166-10C>A
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15766
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30441
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2899
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4176
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1260
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ

17-37786222-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37786222
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37786222
    reference: chr 17
allele count: 1
allele frequency: 8.277186418792524e-6
allele num: 120814
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.266-3C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.166-3C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.157-3C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.58-3C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.166-3C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.58-3C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.190-3C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+407C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+739C>T
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30428
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15864
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7818
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2902
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3397
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2919
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.75e1
  variant carriers: 0
hgvs: c.166-3C>T
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

17-37786240-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37786240
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37786240
    reference: chr 17
allele count: 1
allele frequency: 8.26405302216419e-6
allele num: 121006
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.181G>A
  hgvsp: ENSP00000254079.4:p.Gly61Arg
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.73G>A
  hgvsp: ENSP00000377808.1:p.Gly25Arg
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.172G>A
  hgvsp: ENSP00000462522.1:p.Gly58Arg
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+425G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.205G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.181G>A
  hgvsp: ENSP00000462137.1:p.Gly61Arg
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.281G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.73G>A
  hgvsp: ENSP00000377810.2:p.Gly25Arg
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+757G>A
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30469
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15958
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2905
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4173
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1262
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34615
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly61Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/17-37786249-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37786249
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37786249
    reference: chr 17
allele count: 1
allele frequency: 8.260912665631299e-6
allele num: 121052
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.181C>A
  hgvsp: ENSP00000462522.1:p.Leu61Ile
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.214C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+434C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+766C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.82C>A
  hgvsp: ENSP00000377808.1:p.Leu28Ile
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.190C>A
  hgvsp: ENSP00000462137.1:p.Leu64Ile
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.190C>A
  hgvsp: ENSP00000254079.4:p.Leu64Ile
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.290C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.82C>A
  hgvsp: ENSP00000377810.2:p.Leu28Ile
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: missense
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2899
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7825
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15987
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2918
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu64Ile
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

17-37786256-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37786256
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37786256
    reference: chr 17
allele count: 7
allele frequency: 5.781874648957611e-5
allele num: 121068
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.89C>T
  hgvsp: ENSP00000377808.1:p.Ser30Leu
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+441C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.197C>T
  hgvsp: ENSP00000254079.4:p.Ser66Leu
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.188C>T
  hgvsp: ENSP00000462522.1:p.Ser63Leu
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.221C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.89C>T
  hgvsp: ENSP00000377810.2:p.Ser30Leu
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.197C>T
  hgvsp: ENSP00000462137.1:p.Ser66Leu
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.297C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+773C>T
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7824
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30468
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1261
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34652
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3402
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser66Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

17-37786257-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37786257
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37786257
    reference: chr 17
allele count: 3
allele frequency: 2.477823479855295e-5
allele num: 121074
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.189G>A
  hgvsp: ENST00000582680.1:c.189G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.298G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.90G>A
  hgvsp: ENST00000394267.2:c.90G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.222G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+442G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+774G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.198G>A
  hgvsp: ENST00000580825.1:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.90G>A
  hgvsp: ENST00000394265.1:c.90G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.198G>A
  hgvsp: ENST00000254079.4:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7826
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16001
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30472
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1261
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser66Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

17-37786270-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37786270
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37786270
    reference: chr 17
allele count: 28
allele frequency: 2.312406058503873e-4
allele num: 121086
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.311C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.211C>T
  hgvsp: ENSP00000462137.1:p.Pro71Ser
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.202C>T
  hgvsp: ENSP00000462522.1:p.Pro68Ser
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+787C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.211C>T
  hgvsp: ENSP00000254079.4:p.Pro71Ser
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.103C>T
  hgvsp: ENSP00000377810.2:p.Pro35Ser
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.235C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+455C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.103C>T
  hgvsp: ENSP00000377808.1:p.Pro35Ser
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15993
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7823
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30448
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3397
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34651
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro71Ser
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

17-37786293-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37786293
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37786293
    reference: chr 17
allele count: 1
allele frequency: 8.26296045347127e-6
allele num: 121022
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+810G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.234G>A
  hgvsp: ENST00000254079.4:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.225G>A
  hgvsp: ENST00000582680.1:c.225G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.258G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.334G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.234G>A
  hgvsp: ENST00000580825.1:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+478G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.126G>A
  hgvsp: ENST00000394267.2:c.126G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.126G>A
  hgvsp: ENST00000394265.1:c.126G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7813
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30328
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15992
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2894
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3380
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4039
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2909
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser78Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD

17-37786296-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37786296
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37786296
    reference: chr 17
allele count: 2
allele frequency: 1.65264671371201e-5
allele num: 121018
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.129G>A
  hgvsp: ENST00000394267.2:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.237G>A
  hgvsp: ENST00000580825.1:c.237G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+813G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.129G>A
  hgvsp: ENST00000394265.1:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.237G>A
  hgvsp: ENST00000254079.4:c.237G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.261G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.337G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+481G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.228G>A
  hgvsp: ENST00000582680.1:c.228G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15987
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30302
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7810
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu79Leu
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

17-37786304-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37786304
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37786304
    reference: chr 17
allele count: 2
allele frequency: 1.653548515113433e-5
allele num: 120952
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.133+4C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.232+4C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+489C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.265+4C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.241+4C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.241+4C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.133+4C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.345C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+821C>G
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2889
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15960
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30115
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7793
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
hgvs: c.241+4C>G
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

17-37786307-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37786307
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37786307
    reference: chr 17
allele count: 2
allele frequency: 1.653657891255457e-5
allele num: 120944
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.348T>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.265+7T>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.133+7T>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+492T>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.241+7T>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.241+7T>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.133+7T>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.232+7T>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+824T>A
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7777
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2890
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8386
  bin: 6.75e1
  variant carriers: 0
hgvs: c.241+7T>A
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

17-37786307-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37786307
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37786307
    reference: chr 17
allele count: 10
allele frequency: 8.268289456277285e-5
allele num: 120944
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.133+7T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+492T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.241+7T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.133+7T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.348T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+824T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.265+7T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.232+7T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.241+7T>C
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7777
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2890
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15925
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3368
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
hgvs: c.241+7T>C
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD

17-37786312-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37786312
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37786312
    reference: chr 17
allele count: 484
allele frequency: 4.003440974060349e-3
allele num: 120896
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.241+12C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.133+12C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.241+12C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+829C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.353C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.265+12C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.232+12C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+497C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.133+12C>T
  variant of: http://identifiers.org/hgnc/9287
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 7758
  bin: 3.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 4.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 5.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 29630
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 15855
  bin: 2.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 4.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.75e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 3.75e1
  variant carriers: 41
genotype quality: GenotypeQuality
  all individuals: 8269
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1236
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 7
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

17-37786316-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37786316
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37786316
    reference: chr 17
allele count: 2
allele frequency: 1.654779831543413e-5
allele num: 120862
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.357C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+833C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.241+16C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+501C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.265+16C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.133+16C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.232+16C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.241+16C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.133+16C>T
  variant of: http://identifiers.org/hgnc/9287
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7798
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15907
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2927
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2899
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4018
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/17-37786328-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37786328
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37786328
    reference: chr 17
allele count: 1
allele frequency: 8.283219853221344e-6
allele num: 120726
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.265+28C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.241+28C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.133+28C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+513C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.133+28C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.232+28C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.369C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+845C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.241+28C>A
  variant of: http://identifiers.org/hgnc/9287
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28319
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15521
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31777
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3319
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 801
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1469
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

17-37786333-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37786333
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37786333
    reference: chr 17
allele count: 5
allele frequency: 4.145043357153516e-5
allele num: 120626
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.133+33C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.374C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+518C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.241+33C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.232+33C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+850C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.133+33C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.241+33C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.265+33C>T
  variant of: http://identifiers.org/hgnc/9287
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2950
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7726
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15420
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27792
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3296
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 848
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 878
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

17-37786334-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37786334
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37786334
    reference: chr 17
allele count: 1
allele frequency: 8.288437629506838e-6
allele num: 120650
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.241+34G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.133+34G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+851G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.265+34G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.133+34G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.375G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.232+34G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.241+34G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+519G>A
  variant of: http://identifiers.org/hgnc/9287
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7715
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15464
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27733
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31244
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 896
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1463
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

17-37786340-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37786340
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37786340
    reference: chr 17
allele count: 4
allele frequency: 3.317519822180938e-5
allele num: 120572
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.133+40T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.133+40T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.265+40T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+857T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.232+40T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.241+40T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.241+40T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+525T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.381T>C
  variant of: http://identifiers.org/hgnc/9287
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7679
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26817
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15097
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3247
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7925
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 645
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3971
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
reference allele: T
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

17-37786341-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37786341
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37786341
    reference: chr 17
allele count: 8
allele frequency: 6.634819532908705e-5
allele num: 120576
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.158+526C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580772
  gene symbol: PPP1R1B
  hgvsc: ENST00000580772.1:n.382C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.265+41C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.232+41C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.142+858C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.133+41C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.133+41C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.241+41C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.241+41C>G
  variant of: http://identifiers.org/hgnc/9287
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26741
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15121
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3242
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7720
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2946
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 663
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 629
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1329
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1460
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

17-37790087-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790087
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790087
    reference: chr 17
allele count: 22
allele frequency: 1.832814036023127e-4
allele num: 120034
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.242-49T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.134-49T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1697T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.159-49T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.143-49T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.233-49T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.134-49T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.266-49T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.242-49T>C
  variant of: http://identifiers.org/hgnc/9287
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13126
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4722
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3954
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4500
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2965
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4802
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4490
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3927
  bin: 8.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1133
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 917
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

17-37790100-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790100
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790100
    reference: chr 17
allele count: 5
allele frequency: 4.163890739506995e-5
allele num: 120080
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.242-36G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.134-36G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.134-36G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.143-36G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.266-36G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.159-36G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1710G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.242-36G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.233-36G>A
  variant of: http://identifiers.org/hgnc/9287
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3446
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13120
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4721
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2965
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3956
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4806
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4504
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4490
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1172
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2713
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

17-37790106-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790106
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790106
    reference: chr 17
allele count: 6
allele frequency: 4.993757802746567e-5
allele num: 120150
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1716C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.134-30C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.266-30C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.242-30C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.159-30C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.233-30C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.134-30C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.143-30C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.242-30C>G
  variant of: http://identifiers.org/hgnc/9287
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4489
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2965
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4504
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4720
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2621
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3956
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13120
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3000
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

17-37790116-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790116
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790116
    reference: chr 17
allele count: 56
allele frequency: 4.656035385868933e-4
allele num: 120274
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.134-20C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.242-20C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.159-20C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.242-20C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.134-20C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.143-20C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1726C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.233-20C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.266-20C>T
  variant of: http://identifiers.org/hgnc/9287
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4487
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4800
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3923
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2364
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3443
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2785
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4498
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13153
  bin: 9.75e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 4719
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3950
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50866
  bin: 9.75e1
  variant carriers: 56
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1011
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum

17-37790118-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790118
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790118
    reference: chr 17
allele count: 4
allele frequency: 3.325684259536399e-5
allele num: 120276
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1728C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.242-18C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.143-18C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.134-18C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.242-18C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.266-18C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.134-18C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.233-18C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.159-18C>G
  variant of: http://identifiers.org/hgnc/9287
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2961
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4493
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13139
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4806
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4499
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2389
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3444
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4721
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3353
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 695
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

17-37790118-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790118
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790118
    reference: chr 17
allele count: 14
allele frequency: 1.16398949083774e-4
allele num: 120276
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.134-18C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.143-18C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.266-18C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.233-18C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1728C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.159-18C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.242-18C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.134-18C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.242-18C>T
  variant of: http://identifiers.org/hgnc/9287
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3444
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4721
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4493
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4499
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2961
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2389
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13139
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4806
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50860
  bin: 9.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 1020
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.75e1
  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: C
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

http://identifiers.org/exac.variant/17-37790122-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790122
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790122
    reference: chr 17
allele count: 1
allele frequency: 8.30827005200977e-6
allele num: 120362
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.233-14C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.242-14C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.242-14C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1732C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.134-14C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.266-14C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.143-14C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.159-14C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.134-14C>A
  variant of: http://identifiers.org/hgnc/9287
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4491
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13129
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4500
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4808
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4723
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 707
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50863
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

17-37790125-CTCT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790125
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790122
    reference: chr 17
allele count: 2
allele frequency: 1.661046791688122e-5
allele num: 120406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.159-10_159-8delTCT
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.242-10_242-8delTCT
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.242-10_242-8delTCT
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.134-10_134-8delTCT
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.143-10_143-8delTCT
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.233-10_233-8delTCT
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.266-10_266-8delTCT
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1736_1738delTCT
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.134-10_134-8delTCT
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4723
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13130
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4500
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3446
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3006
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3624
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1325
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
hgvs: c.242-10_242-8delTCT
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: CTCT
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum

17-37790129-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790129
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790129
    reference: chr 17
allele count: 1
allele frequency: 8.30137304710199e-6
allele num: 120462
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.159-7G>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.242-7G>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.233-7G>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.242-7G>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.134-7G>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.134-7G>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.266-7G>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1739G>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.143-7G>T
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4808
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4500
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3446
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4723
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13130
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50862
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
hgvs: c.242-7G>T
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD

17-37790130-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790130
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790130
    reference: chr 17
allele count: 1
allele frequency: 8.298892927683448e-6
allele num: 120498
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.242-6T>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.134-6T>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.233-6T>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.134-6T>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1740T>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.242-6T>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.143-6T>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.159-6T>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.266-6T>G
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4499
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3446
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4723
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13130
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 853
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50864
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: c.242-6T>G
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

17-37790136-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790136
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790136
    reference: chr 17
allele count: 2
allele frequency: 1.658457303016734e-5
allele num: 120594
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.242C>G
  hgvsp: ENSP00000254079.4:p.Ala81Gly
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1746C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.134C>G
  hgvsp: ENSP00000377808.1:p.Ala45Gly
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.143C>G
  hgvsp: ENSP00000462841.1:p.Ala48Gly
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.266C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.233C>G
  hgvsp: ENSP00000462522.1:p.Ala78Gly
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.134C>G
  hgvsp: ENSP00000377810.2:p.Ala45Gly
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.159C>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.242C>G
  hgvsp: ENSP00000462137.1:p.Ala81Gly
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4721
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2527
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4499
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13131
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala81Gly
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

17-37790140-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790140
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790140
    reference: chr 17
allele count: 3
allele frequency: 2.486201581224206e-5
allele num: 120666
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.163G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.270G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.246G>A
  hgvsp: ENST00000254079.4:c.246G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.237G>A
  hgvsp: ENST00000582680.1:c.237G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.138G>A
  hgvsp: ENST00000394265.1:c.138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.138G>A
  hgvsp: ENST00000394267.2:c.138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1750G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.147G>A
  hgvsp: ENST00000579000.1:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.246G>A
  hgvsp: ENST00000580825.1:c.246G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3155
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4500
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13131
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4721
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3446
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val82Val
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS

http://identifiers.org/exac.variant/17-37790144-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790144
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790144
    reference: chr 17
allele count: 1
allele frequency: 8.282122210995345e-6
allele num: 120742
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.167C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.142C>A
  hgvsp: ENSP00000377810.2:p.Arg48Ser
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1754C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.241C>A
  hgvsp: ENSP00000462522.1:p.Arg81Ser
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.250C>A
  hgvsp: ENSP00000254079.4:p.Arg84Ser
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.142C>A
  hgvsp: ENSP00000377808.1:p.Arg48Ser
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.151C>A
  hgvsp: ENSP00000462841.1:p.Arg51Ser
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.274C>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.250C>A
  hgvsp: ENSP00000462137.1:p.Arg84Ser
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3446
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13133
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4499
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3174
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4721
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 727
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg84Ser
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD

17-37790144-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790144
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790144
    reference: chr 17
allele count: 1
allele frequency: 8.282122210995345e-6
allele num: 120742
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.142C>T
  hgvsp: ENSP00000377808.1:p.Arg48Cys
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.142C>T
  hgvsp: ENSP00000377810.2:p.Arg48Cys
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.241C>T
  hgvsp: ENSP00000462522.1:p.Arg81Cys
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.250C>T
  hgvsp: ENSP00000254079.4:p.Arg84Cys
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1754C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.167C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.274C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.151C>T
  hgvsp: ENSP00000462841.1:p.Arg51Cys
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.250C>T
  hgvsp: ENSP00000462137.1:p.Arg84Cys
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13133
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3174
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4721
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3446
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4499
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 727
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 857
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg84Cys
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: C
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

17-37790145-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790145
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790145
    reference: chr 17
allele count: 1
allele frequency: 8.280064915708939e-6
allele num: 120772
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.242G>A
  hgvsp: ENSP00000462522.1:p.Arg81His
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.143G>A
  hgvsp: ENSP00000377810.2:p.Arg48His
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.168G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.251G>A
  hgvsp: ENSP00000462137.1:p.Arg84His
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.152G>A
  hgvsp: ENSP00000462841.1:p.Arg51His
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1755G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.275G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.251G>A
  hgvsp: ENSP00000254079.4:p.Arg84His
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.143G>A
  hgvsp: ENSP00000377808.1:p.Arg48His
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3174
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13133
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4720
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3446
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4500
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1056
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg84His
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

17-37790145-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790145
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790145
    reference: chr 17
allele count: 2
allele frequency: 1.656012983141788e-5
allele num: 120772
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.143G>T
  hgvsp: ENSP00000377808.1:p.Arg48Leu
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1755G>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.143G>T
  hgvsp: ENSP00000377810.2:p.Arg48Leu
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.251G>T
  hgvsp: ENSP00000254079.4:p.Arg84Leu
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.242G>T
  hgvsp: ENSP00000462522.1:p.Arg81Leu
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.152G>T
  hgvsp: ENSP00000462841.1:p.Arg51Leu
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.168G>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.251G>T
  hgvsp: ENSP00000462137.1:p.Arg84Leu
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.275G>T
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4720
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3174
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4500
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13133
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3446
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50867
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Arg84Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum

17-37790155-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790155
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790155
    reference: chr 17
allele count: 2
allele frequency: 1.654122901331569e-5
allele num: 120910
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.261G>A
  hgvsp: ENST00000254079.4:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.162G>A
  hgvsp: ENST00000579000.1:c.162G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.252G>A
  hgvsp: ENST00000582680.1:c.252G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.178G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.261G>A
  hgvsp: ENST00000580825.1:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1765G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.153G>A
  hgvsp: ENST00000394267.2:c.153G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.153G>A
  hgvsp: ENST00000394265.1:c.153G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.285G>A
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3927
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4500
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13131
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3446
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4720
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu87Glu
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

17-37790158-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790158
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790158
    reference: chr 17
allele count: 1
allele frequency: 8.268426187759421e-6
allele num: 120942
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.165T>C
  hgvsp: ENST00000579000.1:c.165T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.156T>C
  hgvsp: ENST00000394265.1:c.156T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.156T>C
  hgvsp: ENST00000394267.2:c.156T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.264T>C
  hgvsp: ENST00000254079.4:c.264T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.264T>C
  hgvsp: ENST00000580825.1:c.264T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.255T>C
  hgvsp: ENST00000582680.1:c.255T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1768T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.181T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.288T>C
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4720
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2654
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3927
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3446
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4500
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13131
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 859
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser88Ser
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

17-37790180-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790180
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790180
    reference: chr 17
allele count: 2
allele frequency: 1.651227687785869e-5
allele num: 121122
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.203T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.178T>C
  hgvsp: ENST00000394267.2:c.178T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.187T>C
  hgvsp: ENST00000579000.1:c.187T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.286T>C
  hgvsp: ENST00000254079.4:c.286T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.310T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.277T>C
  hgvsp: ENST00000582680.1:c.277T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1790T>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.286T>C
  hgvsp: ENST00000580825.1:c.286T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.178T>C
  hgvsp: ENST00000394265.1:c.178T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3446
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4500
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3927
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13131
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4720
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1462
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 867
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu96Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

17-37790191-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790191
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790191
    reference: chr 17
allele count: 3
allele frequency: 2.475737769855417e-5
allele num: 121176
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.189C>T
  hgvsp: ENST00000394267.2:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.189C>T
  hgvsp: ENST00000394265.1:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.297C>T
  hgvsp: ENST00000254079.4:c.297C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.288C>T
  hgvsp: ENST00000582680.1:c.288C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1801C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.297C>T
  hgvsp: ENST00000580825.1:c.297C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.214C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.198C>T
  hgvsp: ENST00000579000.1:c.198C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.321C>T
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4719
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3927
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2759
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13133
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3446
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4499
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 731
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1473
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn99Asn
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD

17-37790196-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790196
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790196
    reference: chr 17
allele count: 1
allele frequency: 8.250688932525866e-6
allele num: 121202
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.194C>T
  hgvsp: ENSP00000377810.2:p.Ala65Val
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.326C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1806C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.302C>T
  hgvsp: ENSP00000462137.1:p.Ala101Val
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.219C>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.302C>T
  hgvsp: ENSP00000254079.4:p.Ala101Val
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.293C>T
  hgvsp: ENSP00000462522.1:p.Ala98Val
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.203C>T
  hgvsp: ENSP00000462841.1:p.Ala68Val
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.194C>T
  hgvsp: ENSP00000377808.1:p.Ala65Val
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4719
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3927
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2765
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13131
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4500
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 768
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala101Val
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

17-37790205-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790205
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790205
    reference: chr 17
allele count: 1
allele frequency: 8.24783082049421e-6
allele num: 121244
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1815A>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.311A>G
  hgvsp: ENSP00000462137.1:p.Glu104Gly
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.302A>G
  hgvsp: ENSP00000462522.1:p.Glu101Gly
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.203A>G
  hgvsp: ENSP00000377808.1:p.Glu68Gly
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.311A>G
  hgvsp: ENSP00000254079.4:p.Glu104Gly
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.203A>G
  hgvsp: ENSP00000377810.2:p.Glu68Gly
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.212A>G
  hgvsp: ENSP00000462841.1:p.Glu71Gly
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.228A>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.335A>G
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4719
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4500
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2788
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13131
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1484
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 872
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu104Gly
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

17-37790207-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790207
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790207
    reference: chr 17
allele count: 4
allele frequency: 3.299241174529858e-5
allele num: 121240
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1817G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.304G>A
  hgvsp: ENSP00000462522.1:p.Glu102Lys
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.313G>A
  hgvsp: ENSP00000254079.4:p.Glu105Lys
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.313G>A
  hgvsp: ENSP00000462137.1:p.Glu105Lys
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.205G>A
  hgvsp: ENSP00000377810.2:p.Glu69Lys
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.214G>A
  hgvsp: ENSP00000462841.1:p.Glu72Lys
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.205G>A
  hgvsp: ENSP00000377808.1:p.Glu69Lys
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.230G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.337G>A
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13133
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4493
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4499
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4718
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3377
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 772
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu105Lys
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff

17-37790218-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790218
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790218
    reference: chr 17
allele count: 1
allele frequency: 8.24715060946443e-6
allele num: 121254
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.324G>A
  hgvsp: ENST00000254079.4:c.324G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.324G>A
  hgvsp: ENST00000580825.1:c.324G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1828G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.225G>A
  hgvsp: ENST00000579000.1:c.225G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.216G>A
  hgvsp: ENST00000394267.2:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.348G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.241G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.315G>A
  hgvsp: ENST00000582680.1:c.315G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.216G>A
  hgvsp: ENST00000394265.1:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4499
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4719
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13132
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4808
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1492
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu108Leu
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS

17-37790224-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790224
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790224
    reference: chr 17
allele count: 1
allele frequency: 8.246470510621453e-6
allele num: 121264
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.247G>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.222G>C
  hgvsp: ENSP00000377810.2:p.Glu74Asp
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.330G>C
  hgvsp: ENSP00000462137.1:p.Glu110Asp
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.231G>C
  hgvsp: ENSP00000462841.1:p.Glu77Asp
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.354G>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.321G>C
  hgvsp: ENSP00000462522.1:p.Glu107Asp
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1834G>C
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.330G>C
  hgvsp: ENSP00000254079.4:p.Glu110Asp
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.222G>C
  hgvsp: ENSP00000377808.1:p.Glu74Asp
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2809
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4719
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4808
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4499
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13132
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4009
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu110Asp
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

17-37790240-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790240
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790240
    reference: chr 17
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.263T>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1850T>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.238T>A
  hgvsp: ENSP00000377810.2:p.Tyr80Asn
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.370T>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.337T>A
  hgvsp: ENSP00000462522.1:p.Tyr113Asn
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.346T>A
  hgvsp: ENSP00000254079.4:p.Tyr116Asn
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.247T>A
  hgvsp: ENSP00000462841.1:p.Tyr83Asn
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.238T>A
  hgvsp: ENSP00000377808.1:p.Tyr80Asn
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.346T>A
  hgvsp: ENSP00000462137.1:p.Tyr116Asn
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4498
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2840
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13132
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3927
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4719
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Tyr116Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

17-37790257-TGAG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790257
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790254
    reference: chr 17
allele count: 4
allele frequency: 3.297391763115376e-5
allele num: 121308
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.261_263delGGA
  hgvsp: ENSP00000377808.1:p.Glu90del
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.369_371delGGA
  hgvsp: ENSP00000462137.1:p.Glu126del
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.369_371delGGA
  hgvsp: ENSP00000254079.4:p.Glu126del
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.393_395delGGA
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.286_288delGGA
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1873_1875delGGA
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.360_362delGGA
  hgvsp: ENSP00000462522.1:p.Glu123del
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.261_263delGGA
  hgvsp: ENSP00000377810.2:p.Glu90del
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.270_272delGGA
  hgvsp: ENSP00000462841.1:p.Glu93del
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13138
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4491
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4720
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3223
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4495
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3923
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2965
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4022
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu126del
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
reference allele: TGAG
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

17-37790257-TGAGGAGGAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790257
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790248
    reference: chr 17
allele count: 1
allele frequency: 8.24347940778844e-6
allele num: 121308
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.273_281delAGAGGAGGA
  hgvsp: ENSP00000462841.1:p.Glu91_Glu93del
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.396_404delAGAGGAGGA
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.363_371delAGAGGAGGA
  hgvsp: ENSP00000462522.1:p.Glu121_Glu123del
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.264_272delAGAGGAGGA
  hgvsp: ENSP00000377810.2:p.Glu88_Glu90del
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.372_380delAGAGGAGGA
  hgvsp: ENSP00000254079.4:p.Glu124_Glu126del
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.289_297delAGAGGAGGA
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.264_272delAGAGGAGGA
  hgvsp: ENSP00000377808.1:p.Glu88_Glu90del
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.372_380delAGAGGAGGA
  hgvsp: ENSP00000462137.1:p.Glu124_Glu126del
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4495
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4491
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13138
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4720
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3223
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3923
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2965
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50871
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1507
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Glu124_Glu126del
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: TGAGGAGGAA
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

17-37790258-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790258
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790258
    reference: chr 17
allele count: 1
allele frequency: 8.243887157672586e-6
allele num: 121302
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.388G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.256G>A
  hgvsp: ENSP00000377808.1:p.Glu86Lys
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.265G>A
  hgvsp: ENSP00000462841.1:p.Glu89Lys
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.256G>A
  hgvsp: ENSP00000377810.2:p.Glu86Lys
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.364G>A
  hgvsp: ENSP00000462137.1:p.Glu122Lys
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.355G>A
  hgvsp: ENSP00000462522.1:p.Glu119Lys
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1868G>A
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.364G>A
  hgvsp: ENSP00000254079.4:p.Glu122Lys
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.281G>A
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4718
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2964
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4495
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu122Lys
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD

17-37790266-AGAG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790266
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790263
    reference: chr 17
allele count: 2
allele frequency: 1.648424106554134e-5
allele num: 121328
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.279_281delGGA
  hgvsp: ENSP00000462841.1:p.Glu93del
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.378_380delGGA
  hgvsp: ENSP00000462137.1:p.Glu126del
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.270_272delGGA
  hgvsp: ENSP00000377808.1:p.Glu90del
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.369_371delGGA
  hgvsp: ENSP00000462522.1:p.Glu123del
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1882_1884delGGA
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.270_272delGGA
  hgvsp: ENSP00000377810.2:p.Glu90del
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.295_297delGGA
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.378_380delGGA
  hgvsp: ENSP00000254079.4:p.Glu126del
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.402_404delGGA
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2131
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4718
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4495
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13137
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2965
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 731
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu126del
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: AGAG
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

17-37790271-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790271
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790271
    reference: chr 17
allele count: 2
allele frequency: 1.648261084555794e-5
allele num: 121340
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.401A>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.278A>G
  hgvsp: ENSP00000462841.1:p.Glu93Gly
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.377A>G
  hgvsp: ENSP00000254079.4:p.Glu126Gly
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.269A>G
  hgvsp: ENSP00000377810.2:p.Glu90Gly
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.269A>G
  hgvsp: ENSP00000377808.1:p.Glu90Gly
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.368A>G
  hgvsp: ENSP00000462522.1:p.Glu123Gly
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.294A>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.377A>G
  hgvsp: ENSP00000462137.1:p.Glu126Gly
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1881A>G
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3947
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2887
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3223
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4717
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4806
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13137
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3449
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4495
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 891
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu126Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum

17-37790272-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790272
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790272
    reference: chr 17
allele count: 19
allele frequency: 1.565848030328004e-4
allele num: 121340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.295G>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.378G>T
  hgvsp: ENSP00000254079.4:p.Glu126Asp
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.402G>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.369G>T
  hgvsp: ENSP00000462522.1:p.Glu123Asp
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1882G>T
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.270G>T
  hgvsp: ENSP00000377810.2:p.Glu90Asp
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.279G>T
  hgvsp: ENSP00000462841.1:p.Glu93Asp
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.378G>T
  hgvsp: ENSP00000462137.1:p.Glu126Asp
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.270G>T
  hgvsp: ENSP00000377808.1:p.Glu90Asp
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3446
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3943
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4497
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4494
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13143
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2887
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4806
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4715
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Glu126Asp
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

17-37790272-GGAT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790272
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790269
    reference: chr 17
allele count: 3
allele frequency: 2.47239162683369e-5
allele num: 121340
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.375_377delTGA
  hgvsp: ENSP00000462522.1:p.Asp125del
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.301_303delTGA
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.276_278delTGA
  hgvsp: ENSP00000377810.2:p.Asp92del
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.285_287delTGA
  hgvsp: ENSP00000462841.1:p.Asp95del
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1888_1890delTGA
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.276_278delTGA
  hgvsp: ENSP00000377808.1:p.Asp92del
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.384_386delTGA
  hgvsp: ENSP00000462137.1:p.Asp128del
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.384_386delTGA
  hgvsp: ENSP00000254079.4:p.Asp128del
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.408_410delTGA
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3943
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4497
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2887
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4494
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4715
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3446
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4806
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13143
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4029
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp128del
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
reference allele: GGAT
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

17-37790275-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790275
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790275
    reference: chr 17
allele count: 2
allele frequency: 1.648342591524222e-5
allele num: 121334
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.282T>G
  hgvsp: ENSP00000462841.1:p.Asp94Glu
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.381T>G
  hgvsp: ENSP00000254079.4:p.Asp127Glu
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.372T>G
  hgvsp: ENSP00000462522.1:p.Asp124Glu
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.273T>G
  hgvsp: ENSP00000377808.1:p.Asp91Glu
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1885T>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.381T>G
  hgvsp: ENSP00000462137.1:p.Asp127Glu
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.273T>G
  hgvsp: ENSP00000377810.2:p.Asp91Glu
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.298T>G
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.405T>G
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2970
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4715
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2903
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4496
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3945
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3445
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13137
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1100
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asp127Glu
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ

17-37790278-T-TGAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790278
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790281
    reference: chr 17
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: TGAA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.307_309dupAGA
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.390_392dupAGA
  hgvsp: ENSP00000254079.4:p.Glu131dup
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.381_383dupAGA
  hgvsp: ENSP00000462522.1:p.Glu128dup
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.282_284dupAGA
  hgvsp: ENSP00000377810.2:p.Glu95dup
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1894_1896dupAGA
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.414_416dupAGA
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.390_392dupAGA
  hgvsp: ENSP00000462137.1:p.Glu131dup
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.282_284dupAGA
  hgvsp: ENSP00000377808.1:p.Glu95dup
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.291_293dupAGA
  hgvsp: ENSP00000462841.1:p.Glu98dup
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: inframe insertion
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4806
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3947
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4491
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2968
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4496
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2901
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13139
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4716
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3446
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu131dup
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

17-37790278-TGAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37790278
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 37790275
    reference: chr 17
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462841
  ensembl transcript: ENST00000579000
  gene symbol: PPP1R1B
  hgvsc: ENST00000579000.1:c.291_293delAGA
  hgvsp: ENSP00000462841.1:p.Glu102del
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462522
  ensembl transcript: ENST00000582680
  gene symbol: PPP1R1B
  hgvsc: ENST00000582680.1:c.381_383delAGA
  hgvsp: ENSP00000462522.1:p.Glu132del
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377810
  ensembl transcript: ENST00000394267
  gene symbol: PPP1R1B
  hgvsc: ENST00000394267.2:c.282_284delAGA
  hgvsp: ENSP00000377810.2:p.Glu99del
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000254079
  ensembl transcript: ENST00000254079
  gene symbol: PPP1R1B
  hgvsc: ENST00000254079.4:c.390_392delAGA
  hgvsp: ENSP00000254079.4:p.Glu135del
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000583446
  gene symbol: PPP1R1B
  hgvsc: ENST00000583446.1:n.414_416delAGA
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000580029
  gene symbol: PPP1R1B
  hgvsc: ENST00000580029.1:n.1894_1896delAGA
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000131771
  ensembl transcript: ENST00000492037
  gene symbol: PPP1R1B
  hgvsc: ENST00000492037.1:n.307_309delAGA
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000462137
  ensembl transcript: ENST00000580825
  gene symbol: PPP1R1B
  hgvsc: ENST00000580825.1:c.390_392delAGA
  hgvsp: ENSP00000462137.1:p.Glu135del
  variant of: http://identifiers.org/hgnc/9287
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000131771
  ensembl protein: ENSP00000377808
  ensembl transcript: ENST00000394265
  gene symbol: PPP1R1B
  hgvsc: ENST00000394265.1:c.282_284delAGA
  hgvsp: ENSP00000377808.1:p.Glu99del
  variant of: http://identifiers.org/hgnc/9287
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4496
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2901
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13139
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3947
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4491
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4806
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2968
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu135del
num of homozygotes: 0
reference allele: TGAA

GenotypeQuality
all individuals: 95
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6754
bin: 9.75e1
variant carriers: 18

GenotypeQuality
all individuals: 255
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1517
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2326
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4598
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1546
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3438
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3500
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8714
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2163
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 18
allele frequency: 1.570954791412114e-3
allele num: 11458
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10094
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65230
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6412
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e-1

FS
type: SiteQuality
SIO_000300: 3.23e0

DP
type: SiteQuality
SIO_000300: 1.814379e6

QD
type: SiteQuality
SIO_000300: 1.246e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.39e-1

GenotypeQuality
all individuals: 1644
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2346
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21280
bin: 6.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1163
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7109
bin: 9.75e1
variant carriers: 544

GenotypeQuality
all individuals: 2137
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 535
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4561
bin: 7.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3460
bin: 7.25e1
variant carriers: 4

GenotypeQuality
all individuals: 3401
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1531
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 527
allele frequency: 5.219889064976228e-2
allele num: 10096
num of homozygotes: 11

Other
type: Population
allele count: 2
allele frequency: 2.277904328018223e-3
allele num: 878
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.460629921259842e-4
allele num: 16256
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6412
num of homozygotes: 0

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

Latino
type: Population
allele count: 28
allele frequency: 2.445414847161572e-3
allele num: 11450
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.133840397472858e-5
allele num: 65212
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.63e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e0

FS
type: SiteQuality
SIO_000300: 1.325e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.57e-1

DP
type: SiteQuality
SIO_000300: 1.811299e6

QD
type: SiteQuality
SIO_000300: 1.322e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-2

GenotypeQuality
all individuals: 1275
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1542
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2154
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2442
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3422
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1638
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8543
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4531
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20302
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16208
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6396
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11444
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 4.959333465582226e-4
allele num: 10082
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65136
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.934e1

MQRankSum
type: SiteQuality
SIO_000300: -2.93e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.296e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.484e0

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

DP
type: SiteQuality
SIO_000300: 1.798273e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.29e-1

GenotypeQuality
all individuals: 3390
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1445
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2346
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3286
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18267
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2262
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4449
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 927
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1172
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7940
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.67860433687573e-5
allele num: 65116
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.141552511415525e-3
allele num: 876
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11438
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16190
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6384
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10078
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.45e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.6e-1

DP
type: SiteQuality
SIO_000300: 1.778115e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.738e0

QD
type: SiteQuality
SIO_000300: 1.052e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 8.763e0

VQSLOD
type: SiteQuality
SIO_000300: 8.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.0e-2

GenotypeQuality
all individuals: 145
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6639
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 71
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1047
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18952
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1173
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2350
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4408
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3374
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1530
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2147
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6372
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.537137235612395e-5
allele num: 65056
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16150
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10064
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.594e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

FS
type: SiteQuality
SIO_000300: 1.9854e1

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

VQSLOD
type: SiteQuality
SIO_000300: -3.138e0

DP
type: SiteQuality
SIO_000300: 1.776827e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

QD
type: SiteQuality
SIO_000300: 1.177e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.309e0

GenotypeQuality
all individuals: 2573
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18725
bin: 6.25e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1095
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1529
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3257
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16182
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6382
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.536948235583426e-5
allele num: 65064
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10070
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.659999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.067e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.23e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

QD
type: SiteQuality
SIO_000300: 9.57e0

DP
type: SiteQuality
SIO_000300: 1.7735e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.0e-2

GenotypeQuality
all individuals: 511
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4270
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1603
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6777
bin: 9.75e1
variant carriers: 175

GenotypeQuality
all individuals: 15446
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2663
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3314
bin: 8.25e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2503
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1397
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3073
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 4
allele frequency: 3.985651654045437e-4
allele num: 10036
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.277463904582549e-4
allele num: 6372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 25
allele frequency: 3.850181728577589e-4
allele num: 64932
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

Latino
type: Population
allele count: 136
allele frequency: 1.192564012627148e-2
allele num: 11404
num of homozygotes: 1

East Asian
type: Population
allele count: 1
allele frequency: 1.166861143523921e-4
allele num: 8570
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 4.970796570150367e-4
allele num: 16094
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.44e-1

DP
type: SiteQuality
SIO_000300: 1.750898e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.94e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.13e-1

QD
type: SiteQuality
SIO_000300: 1.333e1

GenotypeQuality
all individuals: 810
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1351
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4054
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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
all individuals: 1223
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4333
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6284
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9278
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.326259946949602e-4
allele num: 7540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60662
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10808
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15706
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.100000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.84e0

DP
type: SiteQuality
SIO_000300: 1.336494e6

MQRankSum
type: SiteQuality
SIO_000300: 8.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.5e-2

QD
type: SiteQuality
SIO_000300: 9.220000000000001e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 6116
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2494
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: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2407
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19866
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15872
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6378
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9444
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.293326435592343e-4
allele num: 7732
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61568
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.392106e6

QD
type: SiteQuality
SIO_000300: 1.196e1

FS
type: SiteQuality
SIO_000300: 2.273e0

MQRankSum
type: SiteQuality
SIO_000300: 1.62e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e0

VQSLOD
type: SiteQuality
SIO_000300: -3.02e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e0

GenotypeQuality
all individuals: 2897
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2609
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1881
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variant carriers: 0

GenotypeQuality
all individuals: 1957
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4110
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2550
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11040
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15952
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.090301003344482e-4
allele num: 9568
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62314
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.2174e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.9e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.39e-1

QD
type: SiteQuality
SIO_000300: 1.46e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.76e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.46e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

DP
type: SiteQuality
SIO_000300: 1.45894e6

GenotypeQuality
all individuals: 546
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2218
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2653
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1172
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variant carriers: 0

GenotypeQuality
all individuals: 96
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 625
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
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variant carriers: 0

GenotypeQuality
all individuals: 2954
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1366
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3573
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6426
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11090
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7928
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62540
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.25e-5
allele num: 16000
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.252e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.29e-1

FS
type: SiteQuality
SIO_000300: 3.108e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.34e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.802e0

DP
type: SiteQuality
SIO_000300: 1.475397e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.7e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.215e0

GenotypeQuality
all individuals: 182
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1446
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1476
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4160
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1242
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32241
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3947
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2876
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8470
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11398
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64896
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.125949522175937e-5
allele num: 16324
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.577381e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 1.722e0

VQSLOD
type: SiteQuality
SIO_000300: -2.457e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.572e0

MQRankSum
type: SiteQuality
SIO_000300: 1.51e0

QD
type: SiteQuality
SIO_000300: 5.52e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.03e0

GenotypeQuality
all individuals: 3332
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1153
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4163
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 141
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 32901
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3980
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2898
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11422
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10082
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
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: 890
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.532050496384361e-5
allele num: 65272
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.49e-1

QD
type: SiteQuality
SIO_000300: 1.066e1

VQSLOD
type: SiteQuality
SIO_000300: -2.175e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

DP
type: SiteQuality
SIO_000300: 1.588432e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.432e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.637e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.25e-1

GenotypeQuality
all individuals: 1465
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 64
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4049
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variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 2.75e1
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GenotypeQuality
all individuals: 8327
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 519
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4175
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 3371
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10236
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: 8632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.061157074885596e-5
allele num: 65994
num of homozygotes: 0

Other
type: Population
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South Asian
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VQSLOD
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DP
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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FS
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BaseQRankSum
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MQ
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

African
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allele frequency: 0.0e0
allele num: 10286
num of homozygotes: 0

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

South Asian
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allele frequency: 1.212415130940834e-4
allele num: 16496
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66176
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 900
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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BaseQRankSum
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QD
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MQRankSum
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DP
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MQ
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ReadPosRankSum
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FS
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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allele num: 16498
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
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Other
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QD
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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DP
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FS
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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FS
type: SiteQuality
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QD
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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European (Non-Finnish)
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allele num: 66478
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Latino
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European (Finnish)
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African
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East Asian
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InbreedingCoeff
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MQRankSum
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FS
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QD
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DP
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VQSLOD
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MQ
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

European (Finnish)
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South Asian
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European (Non-Finnish)
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allele num: 66490
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Latino
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African
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Other
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ClippingRankSum
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QD
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MQ
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VQSLOD
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MQRankSum
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ReadPosRankSum
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FS
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InbreedingCoeff
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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Latino
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South Asian
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European (Non-Finnish)
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African
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Other
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QD
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ClippingRankSum
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InbreedingCoeff
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DP
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FS
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VQSLOD
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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African
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Latino
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East Asian
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European (Non-Finnish)
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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MQRankSum
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FS
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ClippingRankSum
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DP
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QD
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MQ
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8408
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504755025881786e-5
allele num: 66456
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -6.24e-1

DP
type: SiteQuality
SIO_000300: 1.617566e6

MQRankSum
type: SiteQuality
SIO_000300: 2.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.36e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-2

BaseQRankSum
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SIO_000300: -2.059e0

FS
type: SiteQuality
SIO_000300: 3.624e0

QD
type: SiteQuality
SIO_000300: 1.148e1

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.669309611293753e-5
allele num: 10342
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504845602841149e-5
allele num: 66452
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
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: -2.94e-1

FS
type: SiteQuality
SIO_000300: 2.004e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.909e0

VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

DP
type: SiteQuality
SIO_000300: 1.617162e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.33e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.342e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.37e-1

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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GenotypeQuality
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GenotypeQuality
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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: 11554
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505933377507379e-5
allele num: 66404
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157675387821255e-4
allele num: 8638
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.614837e6

VQSLOD
type: SiteQuality
SIO_000300: -1.836e0

MQRankSum
type: SiteQuality
SIO_000300: 4.07e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.8065e1

QD
type: SiteQuality
SIO_000300: 6.42e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.505e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.53e-1

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.011957471160507e-5
allele num: 66402
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.61366e6

QD
type: SiteQuality
SIO_000300: 1.166e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.99e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.35e0

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.29e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66402
num of homozygotes: 0

South Asian
type: Population
allele count: 10
allele frequency: 6.062810719049351e-4
allele num: 16494
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
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
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.99e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.29e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

DP
type: SiteQuality
SIO_000300: 1.61366e6

QD
type: SiteQuality
SIO_000300: 1.166e1

GenotypeQuality
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variant carriers: 470

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

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

African
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allele count: 446
allele frequency: 4.313346228239845e-2
allele num: 10340
num of homozygotes: 6

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.054884113445252e-4
allele num: 66358
num of homozygotes: 0

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

Latino
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allele count: 27
allele frequency: 2.336853037908949e-3
allele num: 11554
num of homozygotes: 1

Other
type: Population
allele count: 2
allele frequency: 2.212389380530973e-3
allele num: 904
num of homozygotes: 0

South Asian
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allele frequency: 1.212856276531231e-4
allele num: 16490
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.85e0

InbreedingCoeff
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
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DP
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QD
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.157675387821255e-4
allele num: 8638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507295309296997e-5
allele num: 66344
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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MQRankSum
type: SiteQuality
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ClippingRankSum
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MQ
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DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.799e0

QD
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
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European (Finnish)
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African
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Other
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East Asian
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South Asian
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QD
type: SiteQuality
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InbreedingCoeff
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FS
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VQSLOD
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MQRankSum
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MQ
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DP
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

African
type: Population
allele count: 2
allele frequency: 1.942879347192539e-4
allele num: 10294
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.020600495378481e-5
allele num: 66212
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 6.54e-1

DP
type: SiteQuality
SIO_000300: 1.601807e6

MQRankSum
type: SiteQuality
SIO_000300: 8.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

MQ
type: SiteQuality
SIO_000300: 5.93e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.86e0

QD
type: SiteQuality
SIO_000300: 1.134e1

VQSLOD
type: SiteQuality
SIO_000300: 1.44e0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3977
bin: 7.75e1
variant carriers: 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: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510209012927389e-5
allele num: 66216
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.023e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.989e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.95e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.48e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

QD
type: SiteQuality
SIO_000300: 1.769e1

DP
type: SiteQuality
SIO_000300: 1.601741e6

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

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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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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bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66154
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.63284688441047e-4
allele num: 8634
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: 900
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.592543e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.5e-2

MQRankSum
type: SiteQuality
SIO_000300: -7.76e-1

QD
type: SiteQuality
SIO_000300: 1.642e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.403e0

FS
type: SiteQuality
SIO_000300: 2.931e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 8

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

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

East Asian
type: Population
allele count: 7
allele frequency: 8.113120074177098e-4
allele num: 8628
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66166
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.662508662508663e-5
allele num: 11544
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.59341e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.5e-1

FS
type: SiteQuality
SIO_000300: 1.063e0

QD
type: SiteQuality
SIO_000300: 1.511e1

VQSLOD
type: SiteQuality
SIO_000300: 2.95e0

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.2e-2

GenotypeQuality
all individuals: 50
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 22

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65980
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10108
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16410
num of homozygotes: 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: 22
allele frequency: 2.574906367041198e-3
allele num: 8544
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.431948e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

QD
type: SiteQuality
SIO_000300: 1.406e1

VQSLOD
type: SiteQuality
SIO_000300: 5.36e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.29e0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 813
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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

GenotypeQuality
all individuals: 956
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10120
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 5
allele frequency: 3.044325377496347e-4
allele num: 16424
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.01e-1

DP
type: SiteQuality
SIO_000300: 4.439684e6

MQ
type: SiteQuality
SIO_000300: 5.977e1

QD
type: SiteQuality
SIO_000300: 1.448e1

VQSLOD
type: SiteQuality
SIO_000300: 1.4e0

MQRankSum
type: SiteQuality
SIO_000300: 7.24e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.56e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.88e-1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 6

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: 6
allele frequency: 9.086228306629919e-5
allele num: 66034
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10132
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.137e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.164e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.02e-1

FS
type: SiteQuality
SIO_000300: 1.275e0

VQSLOD
type: SiteQuality
SIO_000300: 9.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.71e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

DP
type: SiteQuality
SIO_000300: 4.444512e6

MQ
type: SiteQuality
SIO_000300: 5.965e1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10146
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 55
allele frequency: 8.318712565793454e-4
allele num: 66116
num of homozygotes: 0

Latino
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allele frequency: 8.692628650904033e-5
allele num: 11504
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.75e-1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.957e1

DP
type: SiteQuality
SIO_000300: 4.450967e6

QD
type: SiteQuality
SIO_000300: 1.267e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.43e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 720
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GenotypeQuality
all individuals: 50860
bin: 9.75e1
variant carriers: 4

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
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: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10146
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.049606775559588e-5
allele num: 66120
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -5.639999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.252e1

DP
type: SiteQuality
SIO_000300: 4.450986e6

FS
type: SiteQuality
SIO_000300: 1.186e0

MQRankSum
type: SiteQuality
SIO_000300: -1.89e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.952e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.576e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.54e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 720
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GenotypeQuality
all individuals: 565
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variant carriers: 0

GenotypeQuality
all individuals: 17
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GenotypeQuality
all individuals: 197
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variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 459
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variant carriers: 0

GenotypeQuality
all individuals: 850
bin: 8.25e1
variant carriers: 0

African
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allele count: 9
allele frequency: 8.870490833826139e-4
allele num: 10146
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.537205081669691e-5
allele num: 66120
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.69414014953921e-5
allele num: 11502
num of homozygotes: 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: 1
allele frequency: 1.168770453482936e-4
allele num: 8556
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.639999999999999e-1

DP
type: SiteQuality
SIO_000300: 4.450986e6

MQ
type: SiteQuality
SIO_000300: 5.952e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.576e0

MQRankSum
type: SiteQuality
SIO_000300: -1.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

FS
type: SiteQuality
SIO_000300: 1.186e0

QD
type: SiteQuality
SIO_000300: 1.252e1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 171
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variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511213201958532e-5
allele num: 66172
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10166
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: 16456
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.338e1

DP
type: SiteQuality
SIO_000300: 4.452768e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.077e0

VQSLOD
type: SiteQuality
SIO_000300: -2.074e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.02e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.59e0

FS
type: SiteQuality
SIO_000300: 1.1927e1

MQ
type: SiteQuality
SIO_000300: 5.934e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.86e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 724
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: 2
allele frequency: 1.965022597759874e-4
allele num: 10178
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66194
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

DP
type: SiteQuality
SIO_000300: 4.453902e6

MQRankSum
type: SiteQuality
SIO_000300: -2.262e0

VQSLOD
type: SiteQuality
SIO_000300: 1.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

FS
type: SiteQuality
SIO_000300: 3.439e0

QD
type: SiteQuality
SIO_000300: 1.542e1

MQ
type: SiteQuality
SIO_000300: 5.82e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.006e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 30
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GenotypeQuality
all individuals: 1038
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.076810889645114e-5
allele num: 16456
num of homozygotes: 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: 10190
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66234
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.32e-1

MQ
type: SiteQuality
SIO_000300: 5.947e1

VQSLOD
type: SiteQuality
SIO_000300: -9.525e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.639e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.67e0

DP
type: SiteQuality
SIO_000300: 4.455055e6

QD
type: SiteQuality
SIO_000300: 1.622e1

GenotypeQuality
all individuals: 464
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variant carriers: 0

GenotypeQuality
all individuals: 152
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 1343
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 150
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GenotypeQuality
all individuals: 18
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.805844283192783e-5
allele num: 10198
num of homozygotes: 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: 8572
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66254
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.48e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.71e-1

FS
type: SiteQuality
SIO_000300: 2.676e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

VQSLOD
type: SiteQuality
SIO_000300: 1.56e0

QD
type: SiteQuality
SIO_000300: 1.003e1

MQRankSum
type: SiteQuality
SIO_000300: 2.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

DP
type: SiteQuality
SIO_000300: 4.455314e6

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

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

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

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

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

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

European (Finnish)
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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: 10214
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.015954398769491e-5
allele num: 66314
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

BaseQRankSum
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SIO_000300: -1.004e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

FS
type: SiteQuality
SIO_000300: 1.615e0

ReadPosRankSum
type: SiteQuality
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QD
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ClippingRankSum
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MQRankSum
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 4.456846e6

GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

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

East Asian
type: Population
allele count: 3
allele frequency: 3.497318722312894e-4
allele num: 8578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
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QD
type: SiteQuality
SIO_000300: 1.177e1

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

VQSLOD
type: SiteQuality
SIO_000300: 6.69e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -5.806e0

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.24e-1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.665511265164645e-5
allele num: 11540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66394
num of homozygotes: 0

African
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allele count: 0
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East Asian
type: Population
allele count: 0
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
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MQRankSum
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FS
type: SiteQuality
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DP
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MQ
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 349
bin: 2.25e1
variant carriers: 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: 1
allele frequency: 1.506160195198361e-5
allele num: 66394
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10248
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

DP
type: SiteQuality
SIO_000300: 4.459046e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.24e-1

FS
type: SiteQuality
SIO_000300: 5.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.23e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.33e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

VQSLOD
type: SiteQuality
SIO_000300: 3.15e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.17e-1

QD
type: SiteQuality
SIO_000300: 1.201e1

GenotypeQuality
all individuals: 467
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3817
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 334
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50867
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 857
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 730
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505978735580254e-5
allele num: 66402
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10260
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.84e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.600000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

QD
type: SiteQuality
SIO_000300: 1.204e1

FS
type: SiteQuality
SIO_000300: 1.347e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.95e0

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

DP
type: SiteQuality
SIO_000300: 4.459467e6

MQ
type: SiteQuality
SIO_000300: 5.965e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.31e-1

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

GenotypeQuality
all individuals: 96
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 727
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.949317738791423e-4
allele num: 10260
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66402
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.95e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

DP
type: SiteQuality
SIO_000300: 4.459467e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.600000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.31e-1

QD
type: SiteQuality
SIO_000300: 1.204e1

FS
type: SiteQuality
SIO_000300: 1.347e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.84e-1

GenotypeQuality
all individuals: 50870
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 739
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1067
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 728
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 859
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
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: 6604
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.942124684404739e-4
allele num: 10298
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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: 16490
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -7.781e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.15e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

FS
type: SiteQuality
SIO_000300: 1.3224e1

DP
type: SiteQuality
SIO_000300: 4.461479e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.243e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

QD
type: SiteQuality
SIO_000300: 1.254e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.297e0

GenotypeQuality
all individuals: 61
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 728
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
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: 8590
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: 1
allele frequency: 1.504121292341014e-5
allele num: 66484
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.71e0

DP
type: SiteQuality
SIO_000300: 4.462094e6

FS
type: SiteQuality
SIO_000300: 2.34e0

MQ
type: SiteQuality
SIO_000300: 5.992e1

MQRankSum
type: SiteQuality
SIO_000300: -4.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.649999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.311e1

GenotypeQuality
all individuals: 50872
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
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variant carriers: 0

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

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 757
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.653513326410523e-5
allele num: 11556
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: 10340
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: 8606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501456412720339e-5
allele num: 66602
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.09e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.476e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQ
type: SiteQuality
SIO_000300: 5.97e1

VQSLOD
type: SiteQuality
SIO_000300: 3.65e0

DP
type: SiteQuality
SIO_000300: 4.464933e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.27e-1

GenotypeQuality
all individuals: 40
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4113
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 1083
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variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.75e1
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GenotypeQuality
all individuals: 50872
bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 867
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 765
bin: 7.25e1
variant carriers: 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: 0
allele frequency: 0.0e0
allele num: 66632
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.481086098862845e-4
allele num: 8618
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.08e-1

QD
type: SiteQuality
SIO_000300: 1.264e1

MQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 5.984e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.375e0

DP
type: SiteQuality
SIO_000300: 4.465791e6

MQ
type: SiteQuality
SIO_000300: 5.97e1

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

GenotypeQuality
all individuals: 4129
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1082
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 730
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.160092807424594e-4
allele num: 8620
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66640
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.963e1

QD
type: SiteQuality
SIO_000300: 9.99e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.323e0

DP
type: SiteQuality
SIO_000300: 4.465985e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.36e0

MQRankSum
type: SiteQuality
SIO_000300: -1.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-2

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4143
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159017153453871e-4
allele num: 8628
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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BaseQRankSum
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MQRankSum
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QD
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DP
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ReadPosRankSum
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VQSLOD
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FS
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MQ
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InbreedingCoeff
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SIO_000300: 9.0e-4

ClippingRankSum
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SIO_000300: 8.169999999999999e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.00048007681229e-5
allele num: 66656
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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South Asian
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allele num: 16504
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QD
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VQSLOD
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FS
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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DP
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ReadPosRankSum
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MQ
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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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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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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South Asian
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BaseQRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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ClippingRankSum
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DP
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ReadPosRankSum
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MQ
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

African
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allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500105007350515e-5
allele num: 66662
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Other
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Latino
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
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MQ
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BaseQRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 1.499745043342632e-5
allele num: 66678
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
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African
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South Asian
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East Asian
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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DP
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VQSLOD
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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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GenotypeQuality
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GenotypeQuality
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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 num: 66682
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South Asian
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East Asian
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Other
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African
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European (Finnish)
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Latino
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BaseQRankSum
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ReadPosRankSum
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FS
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MQRankSum
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QD
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VQSLOD
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MQ
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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East Asian
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Latino
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South Asian
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European (Finnish)
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European (Non-Finnish)
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QD
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InbreedingCoeff
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DP
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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MQ
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FS
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ClippingRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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African
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Latino
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East Asian
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European (Non-Finnish)
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South Asian
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ReadPosRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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DP
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MQRankSum
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QD
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FS
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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African
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Other
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Latino
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South Asian
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European (Non-Finnish)
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FS
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VQSLOD
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MQ
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BaseQRankSum
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SIO_000300: -8.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.9e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.84e-1

DP
type: SiteQuality
SIO_000300: 4.468689e6

QD
type: SiteQuality
SIO_000300: 1.489e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.07e-1

GenotypeQuality
all individuals: 473
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 807
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4024
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1102
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50874
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1511
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.728309713100588e-4
allele num: 11572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
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: 10394
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.376e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.88e0

QD
type: SiteQuality
SIO_000300: 1.562e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.53e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

DP
type: SiteQuality
SIO_000300: 4.469032e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.5e0

MQRankSum
type: SiteQuality
SIO_000300: 3.38e-1

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 807
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 735
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1513
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1100
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 889
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50877
bin: 9.75e1
variant carriers: 19

GenotypeQuality
all individuals: 33
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4029
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 12
allele frequency: 1.154512218587647e-3
allele num: 10394
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: 7
allele frequency: 1.049380865289479e-4
allele num: 66706
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: 8642
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

FS
type: SiteQuality
SIO_000300: 1.115e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

QD
type: SiteQuality
SIO_000300: 1.428e1

VQSLOD
type: SiteQuality
SIO_000300: 2.22e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.157e0

MQRankSum
type: SiteQuality
SIO_000300: 7.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.748e0

DP
type: SiteQuality
SIO_000300: 4.469826e6

GenotypeQuality
all individuals: 79
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 807
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 889
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1513
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1100
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 735
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50877
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 8.75e1
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: 3
allele frequency: 4.49734656552634e-5
allele num: 66706
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
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: 10394
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.115e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.34e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

QD
type: SiteQuality
SIO_000300: 1.428e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.157e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.22e0

MQRankSum
type: SiteQuality
SIO_000300: 7.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.748e0

DP
type: SiteQuality
SIO_000300: 4.469826e6

GenotypeQuality
all individuals: 41
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 473
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variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 891
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 808
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1518
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50873
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4054
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 735
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
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: 8642
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: 10396
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499250374812594e-5
allele num: 66700
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.57e0

DP
type: SiteQuality
SIO_000300: 4.469008e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: -4.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.1e-2

FS
type: SiteQuality
SIO_000300: 6.129e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.88e0

QD
type: SiteQuality
SIO_000300: 1.161e1

MQ
type: SiteQuality
SIO_000300: 5.841e1

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50877
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 736
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4059
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 473
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1520
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1099
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 893
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 808
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157139551029854e-4
allele num: 8642
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: 10396
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: 6608
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.399999999999999e-1

FS
type: SiteQuality
SIO_000300: 8.972e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.12e-1

MQ
type: SiteQuality
SIO_000300: 5.744e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.04e0

MQRankSum
type: SiteQuality
SIO_000300: 8.31e-1

DP
type: SiteQuality
SIO_000300: 4.469624e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

QD
type: SiteQuality
SIO_000300: 6.36e0