19-6333419-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6333419
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6333419
    reference: chr 19
allele count: 1
allele frequency: 4.265847623922873e-5
allele num: 23442
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167769
  ensembl protein: ENSP00000301452
  ensembl transcript: ENST00000301452
  gene symbol: ACER1
  hgvsc: ENST00000301452.4:c.93+51C>T
  variant of: http://identifiers.org/hgnc/18356
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4439
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25933
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 794
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1269
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 644
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8382
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17945
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7593
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 855
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1763
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9813
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3896
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2082
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1637
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3272
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 266
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 1070
  num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum

19-6333420-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6333420
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6333420
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 23452
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167769
  ensembl protein: ENSP00000301452
  ensembl transcript: ENST00000301452
  gene symbol: ACER1
  hgvsc: ENST00000301452.4:c.93+50C>T
  variant of: http://identifiers.org/hgnc/18356
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25932
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8882
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2175
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9346
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7629
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1639
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 856
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18199
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 793
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3568
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1758
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 1064
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 216
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 266
  num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP

19-6333425-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6333425
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6333425
    reference: chr 19
allele count: 1
allele frequency: 4.274965800273598e-5
allele num: 23392
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167769
  ensembl protein: ENSP00000301452
  ensembl transcript: ENST00000301452
  gene symbol: ACER1
  hgvsc: ENST00000301452.4:c.93+45G>A
  variant of: http://identifiers.org/hgnc/18356
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25673
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4444
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21472
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2984
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7392
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2551
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 804
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6960
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1758
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1606
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11402
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 497
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 804
  bin: 4.75e1
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genotype quality: GenotypeQuality
  all individuals: 106
  bin: 5.75e1
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genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 5.25e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6946
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 268
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 10994
  num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS

19-6333426-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6333426
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6333426
    reference: chr 19
allele count: 1
allele frequency: 4.22904508162057e-5
allele num: 23646
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167769
  ensembl protein: ENSP00000301452
  ensembl transcript: ENST00000301452
  gene symbol: ACER1
  hgvsc: ENST00000301452.4:c.93+44C>T
  variant of: http://identifiers.org/hgnc/18356
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 21774
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2386
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25399
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1231
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
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  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 1629
  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 852
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3282
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 1096
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 642
  num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD

19-6333430-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6333430
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6333430
    reference: chr 19
allele count: 61
allele frequency: 2.563240608454492e-3
allele num: 23798
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167769
  ensembl protein: ENSP00000301452
  ensembl transcript: ENST00000301452
  gene symbol: ACER1
  hgvsc: ENST00000301452.4:c.93+40G>A
  variant of: http://identifiers.org/hgnc/18356
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 22959
  bin: 7.5e0
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24217
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 1.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 1.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 2806
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 8.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1748
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 5007
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1165
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1617
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6052
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 19397
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2142
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15232
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 654
  bin: 9.75e1
  variant carriers: 60
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3193
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 5.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 858
  bin: 6.75e1
  variant carriers: 1
num of homozygotes: 3
population: South Asian
  type: Population
  allele count: 5
  allele frequency: 7.092198581560284e-4
  allele num: 7050
  num of homozygotes: 1
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 640
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3288
  num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

19-6333431-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6333431
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6333431
    reference: chr 19
allele count: 2
allele frequency: 8.314625426124553e-5
allele num: 24054
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167769
  ensembl protein: ENSP00000301452
  ensembl transcript: ENST00000301452
  gene symbol: ACER1
  hgvsc: ENST00000301452.4:c.93+39C>T
  variant of: http://identifiers.org/hgnc/18356
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23384
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1705
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23765
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4511
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1645
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5757
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19347
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4353
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1736
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1825
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16537
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3512
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 902
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1142
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 7.75e1
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genotype quality: GenotypeQuality
  all individuals: 128
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7116
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 1118
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 2
  allele frequency: 1.761804087385483e-4
  allele num: 11352
  num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: DP

19-6333434-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6333434
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6333433
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 24706
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167769
  ensembl protein: ENSP00000301452
  ensembl transcript: ENST00000301452
  gene symbol: ACER1
  hgvsc: ENST00000301452.4:c.93+35delA
  variant of: http://identifiers.org/hgnc/18356
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24740
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4425
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19116
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18861
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1151
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4893
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3649
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 940
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1683
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1073
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1732
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3947
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 290
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 1190
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3350
  num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: AT
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD

19-6333436-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6333436
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6333436
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 24646
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167769
  ensembl protein: ENSP00000301452
  ensembl transcript: ENST00000301452
  gene symbol: ACER1
  hgvsc: ENST00000301452.4:c.93+34G>A
  variant of: http://identifiers.org/hgnc/18356
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4385
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25450
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21662
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3523
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 942
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1691
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1243
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1656
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4473
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18496
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1004
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3378
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4085
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 220
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3360
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7220
  num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD

19-6333439-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6333439
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6333439
    reference: chr 19
allele count: 1
allele frequency: 4.003523100328289e-5
allele num: 24978
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167769
  ensembl protein: ENSP00000301452
  ensembl transcript: ENST00000301452
  gene symbol: ACER1
  hgvsc: ENST00000301452.4:c.93+31C>T
  variant of: http://identifiers.org/hgnc/18356
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26645
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4333
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20352
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1866
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4425
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 971
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1125
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1641
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22088
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1647
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3386
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 220
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 1230
  num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

http://identifiers.org/exac.variant/19-6333440-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6333440
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6333440
    reference: chr 19
allele count: 92
allele frequency: 3.657469984893059e-3
allele num: 25154
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167769
  ensembl protein: ENSP00000301452
  ensembl transcript: ENST00000301452
  gene symbol: ACER1
  hgvsc: ENST00000301452.4:c.93+30G>T
  variant of: http://identifiers.org/hgnc/18356
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 27081
  bin: 7.5e0
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4414
  bin: 1.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 19702
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3849
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2640
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 5.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 5.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 880
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22638
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 7.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 4422
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 141
  bin: 9.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17278
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3591
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 8.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 977
  bin: 6.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1624
  bin: 2.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 9.75e1
  variant carriers: 92
genotype quality: GenotypeQuality
  all individuals: 1622
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 8.25e1
  variant carriers: 3
num of homozygotes: 1
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 708
  num of homozygotes: 0
population: African
  type: Population
  allele count: 90
  allele frequency: 2.601156069364162e-2
  allele num: 3460
  num of homozygotes: 1
population: South Asian
  type: Population
  allele count: 1
  allele frequency: 1.375515818431912e-4
  allele num: 7270
  num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

19-6333440-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6333440
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6333440
    reference: chr 19
allele count: 75
allele frequency: 2.981633139858472e-3
allele num: 25154
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167769
  ensembl protein: ENSP00000301452
  ensembl transcript: ENST00000301452
  gene symbol: ACER1
  hgvsc: ENST00000301452.4:c.93+30G>A
  variant of: http://identifiers.org/hgnc/18356
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3849
  bin: 2.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 1.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 4414
  bin: 1.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19702
  bin: 2.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 27081
  bin: 7.5e0
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 9.75e1
  variant carriers: 78
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22638
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 17278
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3591
  bin: 1.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 5.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1624
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1428
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4422
  bin: 6.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 7.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 9.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 1622
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2640
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 880
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 102
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genotype quality: GenotypeQuality
  all individuals: 977
  bin: 6.75e1
  variant carriers: 2
num of homozygotes: 1
population: South Asian
  type: Population
  allele count: 47
  allele frequency: 6.464924346629986e-3
  allele num: 7270
  num of homozygotes: 1
population: Other
  type: Population
  allele count: 1
  allele frequency: 4.464285714285714e-3
  allele num: 224
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 26
  allele frequency: 2.17828418230563e-3
  allele num: 11936
  num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-6333440-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6333440
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6333440
    reference: chr 19
allele count: 1
allele frequency: 3.975510853144629e-5
allele num: 25154
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167769
  ensembl protein: ENSP00000301452
  ensembl transcript: ENST00000301452
  gene symbol: ACER1
  hgvsc: ENST00000301452.4:c.93+30G>C
  variant of: http://identifiers.org/hgnc/18356
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3849
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19702
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4414
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27081
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1622
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1428
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2640
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1624
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17278
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3591
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 22638
  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 353
  bin: 7.75e1
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genotype quality: GenotypeQuality
  all individuals: 880
  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 141
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 977
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7270
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 11936
  num of homozygotes: 0
population: African
  type: Population
  allele count: 1
  allele frequency: 2.890173410404624e-4
  allele num: 3460
  num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

19-6333441-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6333441
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6333441
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 25562
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167769
  ensembl protein: ENSP00000301452
  ensembl transcript: ENST00000301452
  gene symbol: ACER1
  hgvsc: ENST00000301452.4:c.93+29C>T
  variant of: http://identifiers.org/hgnc/18356
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27800
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4072
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18936
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4764
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16793
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 362
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3274
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1107
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 837
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 23976
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 358
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1033
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1648
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 12114
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 1292
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7378
  num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP

20-9434116-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9434116
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9434116
    reference: chr 20
allele count: 1
allele frequency: 8.982788976321368e-6
allele num: 111324
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.2996+7C>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.2975+7C>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.2960+7C>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.2960+7C>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.2960+7C>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2737+7C>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.2960+7C>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.2996+7C>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2651+7C>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2687+7C>G
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8610
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10798
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21496
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7620
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1721
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 9.25e1
  variant carriers: 0
hgvs: c.2960+7C>G
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP

20-9434117-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9434117
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9434117
    reference: chr 20
allele count: 2
allele frequency: 1.794880999389741e-5
allele num: 111428
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.2996+8T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2737+8T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.2996+8T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2687+8T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.2960+8T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.2975+8T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2651+8T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.2960+8T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.2960+8T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.2960+8T>G
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10827
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21512
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7553
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4624
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8642
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1557
  bin: 3.25e1
  variant carriers: 0
hgvs: c.2960+8T>G
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

20-9434120-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9434120
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9434120
    reference: chr 20
allele count: 4
allele frequency: 3.646640532409518e-5
allele num: 109690
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.2975+11T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.2960+11T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2737+11T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.2960+11T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2687+11T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.2996+11T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.2996+11T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.2960+11T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2651+11T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.2960+11T>C
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10793
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5381
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7006
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19912
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9632
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 871
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

20-9434130-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9434130
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9434130
    reference: chr 20
allele count: 1
allele frequency: 9.578544061302682e-6
allele num: 104400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.2960+21C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2737+21C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.2960+21C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.2960+21C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.2975+21C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.2996+21C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.2960+21C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2651+21C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2687+21C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.2996+21C>T
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3808
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18369
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6791
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7371
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4505
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2961
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

20-9434138-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9434138
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9434138
    reference: chr 20
allele count: 1
allele frequency: 1.008227133408614e-5
allele num: 99184
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.2960+29T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.2975+29T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.2960+29T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2651+29T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.2996+29T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.2960+29T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.2960+29T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2687+29T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.2996+29T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2737+29T>C
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8863
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3895
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6988
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8480
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23446
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1481
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4104
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD

20-9434151-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9434151
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9434151
    reference: chr 20
allele count: 1
allele frequency: 1.07693633152408e-5
allele num: 92856
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.2996+42A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.2960+42A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2687+42A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.2960+42A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.2975+42A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.2996+42A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2737+42A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.2960+42A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.2960+42A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2651+42A>G
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11683
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21726
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12312
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3334
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1862
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4696
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8338
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

20-9434158-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9434158
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9434158
    reference: chr 20
allele count: 1
allele frequency: 1.141682840506907e-5
allele num: 87590
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.2960+49G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.2960+49G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2687+49G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.2975+49G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.2960+49G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2737+49G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2651+49G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.2996+49G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.2960+49G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.2996+49G>A
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4857
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12025
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13676
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19957
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4621
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2624
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5538
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8358
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

20-9438014-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438014
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438014
    reference: chr 20
allele count: 1
allele frequency: 8.479894170920747e-6
allele num: 117926
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.2976-47G>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.2961-47G>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2738-47G>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2652-47G>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.2961-47G>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.2997-47G>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.2961-47G>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2688-47G>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.2961-47G>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.2997-47G>C
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4261
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4959
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9070
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5990
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 931
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4486
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum

20-9438018-AAT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438018
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438016
    reference: chr 20
allele count: 1
allele frequency: 8.462814393554721e-6
allele num: 118164
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2652-40_2652-39delAT
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2688-40_2688-39delAT
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.2961-40_2961-39delAT
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.2961-40_2961-39delAT
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.2997-40_2997-39delAT
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2738-40_2738-39delAT
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.2976-40_2976-39delAT
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.2961-40_2961-39delAT
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.2961-40_2961-39delAT
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.2997-40_2997-39delAT
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2513
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13338
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15501
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9179
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3838
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1506
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3638
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: AAT
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

20-9438021-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438021
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438021
    reference: chr 20
allele count: 197
allele frequency: 1.666694867933468e-3
allele num: 118198
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.2961-40A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.2976-40A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.2997-40A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.2997-40A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.2961-40A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2688-40A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2738-40A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.2961-40A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2652-40A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.2961-40A>G
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4978
  bin: 3.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 4.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 2521
  bin: 4.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 2698
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 16680
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 9269
  bin: 3.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 13485
  bin: 2.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3783
  bin: 1.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1145
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3649
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19472
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 865
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 4
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

20-9438025-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438025
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438025
    reference: chr 20
allele count: 1
allele frequency: 8.45394291897741e-6
allele num: 118288
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2688-36A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.2997-36A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.2997-36A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.2961-36A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.2976-36A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2652-36A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.2961-36A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.2961-36A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.2961-36A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2738-36A>G
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9397
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13749
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17777
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4993
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 736
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3135
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2352
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

20-9438030-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438030
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438030
    reference: chr 20
allele count: 1
allele frequency: 8.440100605999223e-6
allele num: 118482
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.2997-31C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2688-31C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.2961-31C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.2961-31C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.2997-31C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.2961-31C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.2976-31C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2652-31C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.2961-31C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2738-31C>T
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5010
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2376
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9499
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2351
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

20-9438035-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438035
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438035
    reference: chr 20
allele count: 1
allele frequency: 8.405762991106703e-6
allele num: 118966
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2688-26A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.2961-26A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.2976-26A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.2961-26A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.2961-26A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.2997-26A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.2997-26A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2652-26A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2738-26A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.2961-26A>G
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14578
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19847
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9656
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1184
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3209
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3720
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/20-9438039-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438039
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438039
    reference: chr 20
allele count: 1
allele frequency: 8.381667616588997e-6
allele num: 119308
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.2961-22A>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.2961-22A>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.2997-22A>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.2976-22A>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2688-22A>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.2961-22A>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.2997-22A>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2738-22A>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2652-22A>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.2961-22A>C
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5029
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20338
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9743
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14829
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9882
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 504
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3216
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

20-9438050-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438050
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438050
    reference: chr 20
allele count: 1
allele frequency: 8.347384764353328e-6
allele num: 119798
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.2961-11T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.2997-11T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.2997-11T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2652-11T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.2961-11T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2688-11T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.2961-11T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.2961-11T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2738-11T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.2976-11T>G
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9844
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15142
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 784
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP

20-9438053-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438053
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438053
    reference: chr 20
allele count: 3
allele frequency: 2.501292334372759e-5
allele num: 119938
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2652-8A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.2961-8A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2688-8A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.2976-8A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.2997-8A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2738-8A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.2961-8A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.2961-8A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.2997-8A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.2961-8A>G
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9860
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20743
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15220
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3246
  bin: 7.25e1
  variant carriers: 0
hgvs: c.2961-8A>G
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

20-9438055-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438055
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438055
    reference: chr 20
allele count: 133
allele frequency: 1.108444177751108e-3
allele num: 119988
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.2961-6T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.2997-6T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2652-6T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2688-6T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2738-6T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.2976-6T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.2961-6T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.2961-6T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.2961-6T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.2997-6T>C
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9849
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 20742
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15212
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 4.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 5.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 4.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 6.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 7652
  bin: 6.75e1
  variant carriers: 0
hgvs: c.2961-6T>C
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

20-9438076-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438076
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438076
    reference: chr 20
allele count: 4
allele frequency: 3.319171534784917e-5
allele num: 120512
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.2991C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.2976C>T
  hgvsp: ENST00000334005.3:c.2976C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3012C>T
  hgvsp: ENST00000378473.3:c.3012C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2703C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3012C>T
  hgvsp: ENST00000414679.2:c.3012C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.2976C>T
  hgvsp: ENST00000278655.4:c.2976C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.2976C>T
  hgvsp: ENST00000378493.1:c.2976C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.2976C>T
  hgvsp: ENST00000378501.2:c.2976C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2753C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2667C>T
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5053
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9949
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15577
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20841
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu992Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

20-9438077-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438077
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438077
    reference: chr 20
allele count: 11
allele frequency: 9.126661467235286e-5
allele num: 120526
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3013G>A
  hgvsp: ENSP00000367734.3:p.Glu1005Lys
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.2977G>A
  hgvsp: ENSP00000334105.3:p.Glu993Lys
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.2977G>A
  hgvsp: ENSP00000367762.2:p.Glu993Lys
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2754G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.2977G>A
  hgvsp: ENSP00000278655.4:p.Glu993Lys
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.2977G>A
  hgvsp: ENSP00000367754.1:p.Glu993Lys
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2668G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3013G>A
  hgvsp: ENSP00000390616.2:p.Glu1005Lys
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2704G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.2992G>A
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5053
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9960
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20838
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4699
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Glu993Lys
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

20-9438082-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438082
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438082
    reference: chr 20
allele count: 1
allele frequency: 8.293799555452344e-6
allele num: 120572
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3018G>A
  hgvsp: ENSP00000390616.2:p.Met1006Ile
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.2997G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3018G>A
  hgvsp: ENSP00000367734.3:p.Met1006Ile
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.2982G>A
  hgvsp: ENSP00000278655.4:p.Met994Ile
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.2982G>A
  hgvsp: ENSP00000367762.2:p.Met994Ile
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2759G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.2982G>A
  hgvsp: ENSP00000367754.1:p.Met994Ile
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2673G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2709G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.2982G>A
  hgvsp: ENSP00000334105.3:p.Met994Ile
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20876
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15662
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5054
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9957
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Met994Ile
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

20-9438083-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438083
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438083
    reference: chr 20
allele count: 1
allele frequency: 8.291186468783682e-6
allele num: 120610
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.2983A>G
  hgvsp: ENSP00000334105.3:p.Lys995Glu
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3019A>G
  hgvsp: ENSP00000390616.2:p.Lys1007Glu
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.2983A>G
  hgvsp: ENSP00000367754.1:p.Lys995Glu
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.2983A>G
  hgvsp: ENSP00000367762.2:p.Lys995Glu
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2710A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.2998A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2760A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.2983A>G
  hgvsp: ENSP00000278655.4:p.Lys995Glu
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3019A>G
  hgvsp: ENSP00000367734.3:p.Lys1007Glu
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2674A>G
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5051
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9955
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15680
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26292
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Lys995Glu
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

20-9438092-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438092
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438092
    reference: chr 20
allele count: 212
allele frequency: 1.756537301560998e-3
allele num: 120692
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3007A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2769A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.2992A>G
  hgvsp: ENSP00000367754.1:p.Thr998Ala
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2719A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.2992A>G
  hgvsp: ENSP00000367762.2:p.Thr998Ala
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.2992A>G
  hgvsp: ENSP00000334105.3:p.Thr998Ala
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.2992A>G
  hgvsp: ENSP00000278655.4:p.Thr998Ala
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3028A>G
  hgvsp: ENSP00000367734.3:p.Thr1010Ala
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2683A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3028A>G
  hgvsp: ENSP00000390616.2:p.Thr1010Ala
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15659
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 5.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 9930
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 5057
  bin: 3.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 2552
  bin: 4.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 9.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20859
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 5.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr998Ala
num of homozygotes: 3
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

20-9438093-CAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438093
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438091
    reference: chr 20
allele count: 3
allele frequency: 2.485871961021528e-5
allele num: 120682
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3031_3032delGA
  hgvsp: ENSP00000367734.3:p.Glu1011AsnfsTer13
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2686_2687delGA
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2722_2723delGA
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.2995_2996delGA
  hgvsp: ENSP00000367762.2:p.Glu999AsnfsTer13
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3031_3032delGA
  hgvsp: ENSP00000390616.2:p.Glu1011AsnfsTer13
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3010_3011delGA
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2772_2773delGA
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.2995_2996delGA
  hgvsp: ENSP00000334105.3:p.Glu999AsnfsTer13
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.2995_2996delGA
  hgvsp: ENSP00000278655.4:p.Glu999AsnfsTer13
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.2995_2996delGA
  hgvsp: ENSP00000367754.1:p.Glu999AsnfsTer13
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20866
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15738
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5058
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10004
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu999AsnfsTer13
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: CAG
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum

http://identifiers.org/exac.variant/20-9438096-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438096
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438096
    reference: chr 20
allele count: 1
allele frequency: 8.285004142502071e-6
allele num: 120700
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2773A>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.2996A>C
  hgvsp: ENSP00000367762.2:p.Glu999Ala
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.2996A>C
  hgvsp: ENSP00000278655.4:p.Glu999Ala
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2687A>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3011A>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2723A>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.2996A>C
  hgvsp: ENSP00000367754.1:p.Glu999Ala
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3032A>C
  hgvsp: ENSP00000367734.3:p.Glu1011Ala
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.2996A>C
  hgvsp: ENSP00000334105.3:p.Glu999Ala
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3032A>C
  hgvsp: ENSP00000390616.2:p.Glu1011Ala
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20876
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5057
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu999Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/20-9438100-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438100
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438100
    reference: chr 20
allele count: 8
allele frequency: 6.627344423089668e-5
allele num: 120712
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3015C>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3036C>A
  hgvsp: ENST00000414679.2:c.3036C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2727C>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2691C>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3000C>A
  hgvsp: ENST00000334005.3:c.3000C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3000C>A
  hgvsp: ENST00000378501.2:c.3000C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3000C>A
  hgvsp: ENST00000278655.4:c.3000C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3036C>A
  hgvsp: ENST00000378473.3:c.3036C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3000C>A
  hgvsp: ENST00000378493.1:c.3000C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2777C>A
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15775
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10011
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5058
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9900
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ile1000Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

20-9438109-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438109
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438109
    reference: chr 20
allele count: 824
allele frequency: 6.823112465429011e-3
allele num: 120766
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3009G>A
  hgvsp: ENST00000378493.1:c.3009G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3009G>A
  hgvsp: ENST00000334005.3:c.3009G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2700G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2786G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3009G>A
  hgvsp: ENST00000378501.2:c.3009G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3045G>A
  hgvsp: ENST00000414679.2:c.3045G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3009G>A
  hgvsp: ENST00000278655.4:c.3009G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3045G>A
  hgvsp: ENST00000378473.3:c.3045G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3024G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2736G>A
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 5.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.25e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 15692
  bin: 2.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 4.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 20607
  bin: 2.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9905
  bin: 3.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 5016
  bin: 3.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 4.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 5.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 9.75e1
  variant carriers: 189
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 7.25e1
  variant carriers: 51
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 1
hgvs: p.Gln1003Gln
num of homozygotes: 33
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

20-9438111-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438111
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438111
    reference: chr 20
allele count: 9
allele frequency: 7.452798940046373e-5
allele num: 120760
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2738C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2702C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3047C>T
  hgvsp: ENSP00000367734.3:p.Thr1016Met
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3011C>T
  hgvsp: ENSP00000278655.4:p.Thr1004Met
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3011C>T
  hgvsp: ENSP00000367762.2:p.Thr1004Met
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2788C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3026C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3011C>T
  hgvsp: ENSP00000367754.1:p.Thr1004Met
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3011C>T
  hgvsp: ENSP00000334105.3:p.Thr1004Met
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3047C>T
  hgvsp: ENSP00000390616.2:p.Thr1016Met
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10043
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5090
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20629
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr1004Met
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

20-9438112-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438112
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438112
    reference: chr 20
allele count: 4
allele frequency: 3.312464805061446e-5
allele num: 120756
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3012G>A
  hgvsp: ENST00000378493.1:c.3012G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3012G>A
  hgvsp: ENST00000334005.3:c.3012G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3048G>A
  hgvsp: ENST00000414679.2:c.3048G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2739G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3012G>A
  hgvsp: ENST00000278655.4:c.3012G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2703G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3048G>A
  hgvsp: ENST00000378473.3:c.3048G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3012G>A
  hgvsp: ENST00000378501.2:c.3012G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3027G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2789G>A
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5091
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15869
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10045
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3254
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr1004Thr
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum

20-9438115-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438115
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438115
    reference: chr 20
allele count: 5
allele frequency: 4.14003245785447e-5
allele num: 120772
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2706G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3015G>A
  hgvsp: ENST00000378501.2:c.3015G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3030G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3015G>A
  hgvsp: ENST00000278655.4:c.3015G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3015G>A
  hgvsp: ENST00000378493.1:c.3015G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3051G>A
  hgvsp: ENST00000414679.2:c.3051G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3015G>A
  hgvsp: ENST00000334005.3:c.3015G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3051G>A
  hgvsp: ENST00000378473.3:c.3051G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2792G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2742G>A
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5091
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20624
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10034
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15883
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu1005Leu
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum

20-9438122-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438122
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438122
    reference: chr 20
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3022G>C
  hgvsp: ENSP00000367754.1:p.Asp1008His
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3022G>C
  hgvsp: ENSP00000367762.2:p.Asp1008His
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3058G>C
  hgvsp: ENSP00000367734.3:p.Asp1020His
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3022G>C
  hgvsp: ENSP00000278655.4:p.Asp1008His
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2749G>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3022G>C
  hgvsp: ENSP00000334105.3:p.Asp1008His
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2799G>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3037G>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3058G>C
  hgvsp: ENSP00000390616.2:p.Asp1020His
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2713G>C
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15894
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10030
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20578
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5088
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26433
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp1008His
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum

20-9438134-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438134
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438134
    reference: chr 20
allele count: 4
allele frequency: 3.31389183457052e-5
allele num: 120704
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2761A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3034A>G
  hgvsp: ENSP00000278655.4:p.Lys1012Glu
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3034A>G
  hgvsp: ENSP00000367754.1:p.Lys1012Glu
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3034A>G
  hgvsp: ENSP00000367762.2:p.Lys1012Glu
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3070A>G
  hgvsp: ENSP00000367734.3:p.Lys1024Glu
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3034A>G
  hgvsp: ENSP00000334105.3:p.Lys1012Glu
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2725A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2811A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3049A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3070A>G
  hgvsp: ENSP00000390616.2:p.Lys1024Glu
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5092
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20363
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15912
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Lys1012Glu
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

20-9438153-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438153
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438153
    reference: chr 20
allele count: 1
allele frequency: 8.292836647703714e-6
allele num: 120586
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3036+17T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3051+17T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3072+17T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2813+17T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3036+17T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3036+17T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3072+17T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2727+17T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2763+17T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3036+17T>G
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15885
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10015
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5090
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19556
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2584
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9858
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 25423
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum

20-9438158-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438158
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438158
    reference: chr 20
allele count: 1
allele frequency: 8.296964970213896e-6
allele num: 120526
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3036+22C>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2813+22C>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2763+22C>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3051+22C>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3036+22C>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3072+22C>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3036+22C>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2727+22C>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3072+22C>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3036+22C>G
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10030
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19090
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2591
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15814
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5091
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

20-9438164-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438164
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438164
    reference: chr 20
allele count: 206
allele frequency: 1.710906614398193e-3
allele num: 120404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2763+28T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2813+28T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3036+28T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3072+28T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3072+28T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3036+28T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3036+28T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2727+28T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3051+28T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3036+28T>C
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 8.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 5.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18077
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 4.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 9972
  bin: 3.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 15675
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 6.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 5.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 4.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 5078
  bin: 3.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 9.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 6.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 2358
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1677
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 478
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

20-9438169-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438169
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438169
    reference: chr 20
allele count: 1
allele frequency: 8.31282835672009e-6
allele num: 120296
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3072+33T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3036+33T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2727+33T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3072+33T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2763+33T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3051+33T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3036+33T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2813+33T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3036+33T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3036+33T>G
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2593
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15429
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16992
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9967
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 656
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3727
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: T
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

20-9438172-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438172
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438172
    reference: chr 20
allele count: 11007
allele frequency: 9.163184096168894e-2
allele num: 120122
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3036+36A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2813+36A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3072+36A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2727+36A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2763+36A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3036+36A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3036+36A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3051+36A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3072+36A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3036+36A>G
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 8.25e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 13798
  bin: 2.25e1
  variant carriers: 582
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 5.75e1
  variant carriers: 711
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.5e0
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 13574
  bin: 2.75e1
  variant carriers: 847
genotype depth: GenotypeDepth
  all individuals: 5607
  bin: 3.75e1
  variant carriers: 1469
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2945
  bin: 1.75e1
  variant carriers: 336
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 1.25e1
  variant carriers: 124
genotype depth: GenotypeDepth
  all individuals: 3433
  bin: 4.25e1
  variant carriers: 1331
genotype depth: GenotypeDepth
  all individuals: 9411
  bin: 3.25e1
  variant carriers: 1159
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 6.25e1
  variant carriers: 479
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 5.25e1
  variant carriers: 919
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 6.75e1
  variant carriers: 308
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.25e1
  variant carriers: 197
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 9.75e1
  variant carriers: 380
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.75e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.75e1
  variant carriers: 125
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 4.75e1
  variant carriers: 1222
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.5e0
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 7.5e0
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 700
  bin: 2.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 2599
  bin: 7.25e1
  variant carriers: 23
num of homozygotes: 568
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

20-9438177-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438177
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438177
    reference: chr 20
allele count: 3
allele frequency: 2.501876407305479e-5
allele num: 119910
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3036+41A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2813+41A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3036+41A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2727+41A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3036+41A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3036+41A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3072+41A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3051+41A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2763+41A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3072+41A>G
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5804
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14107
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2696
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10221
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12687
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2923
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5440
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1583
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4502
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17337
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

20-9438179-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438179
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438179
    reference: chr 20
allele count: 1
allele frequency: 8.344041519950603e-6
allele num: 119846
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3036+43A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3036+43A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3036+43A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3072+43A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2813+43A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3036+43A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2727+43A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3072+43A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3051+43A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2763+43A>G
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5799
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12978
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2685
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10119
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5443
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1044
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2313
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2103
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum

20-9438183-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9438183
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9438183
    reference: chr 20
allele count: 1
allele frequency: 8.369601606963508e-6
allele num: 119480
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3051+47T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2813+47T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3072+47T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3072+47T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2727+47T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3036+47T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3036+47T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3036+47T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3036+47T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2763+47T>C
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2632
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2902
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5756
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9545
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13295
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14239
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4406
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2925
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/20-9440242-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9440242
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9440242
    reference: chr 20
allele count: 1
allele frequency: 8.928730870194111e-6
allele num: 111998
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2728-40A>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3037-40A>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3073-40A>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3037-40A>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3073-40A>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3037-40A>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3037-40A>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3051+2106A>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2814-40A>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2764-40A>C
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5288
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14335
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3621
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8641
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4439
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3450
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

20-9440244-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9440244
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9440244
    reference: chr 20
allele count: 1
allele frequency: 8.927774305865547e-6
allele num: 112010
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3051+2108G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3073-38G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2728-38G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3073-38G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2764-38G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2814-38G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3037-38G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3037-38G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3037-38G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3037-38G>A
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24140
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14520
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8199
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4806
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2057
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1438
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

20-9440257-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9440257
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9440257
    reference: chr 20
allele count: 2
allele frequency: 1.765443214519005e-5
allele num: 113286
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3037-25G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3037-25G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2728-25G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3073-25G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3073-25G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3037-25G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3051+2121G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2764-25G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2814-25G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3037-25G>A
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29310
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15847
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3763
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4778
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1400
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

20-9440261-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9440261
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9440261
    reference: chr 20
allele count: 3
allele frequency: 2.630840465834152e-5
allele num: 114032
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2728-21C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2764-21C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3037-21C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3037-21C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3073-21C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3073-21C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3037-21C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2814-21C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3051+2125C>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3037-21C>T
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16442
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3828
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3959
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 685
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1607
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1281
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1082
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

20-9440262-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9440262
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9440262
    reference: chr 20
allele count: 7
allele frequency: 6.114498349085445e-5
allele num: 114482
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2814-20G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2764-20G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3073-20G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3037-20G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3051+2126G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3073-20G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3037-20G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3037-20G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3037-20G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2728-20G>A
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30681
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4036
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3460
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16602
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1200
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5407
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42691
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1444
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

20-9440272-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9440272
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9440272
    reference: chr 20
allele count: 1
allele frequency: 8.573829243616784e-6
allele num: 116634
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3037-10T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3037-10T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3073-10T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3051+2136T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2764-10T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3037-10T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3073-10T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3037-10T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2814-10T>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2728-10T>G
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31803
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18048
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP

20-9440292-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9440292
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9440292
    reference: chr 20
allele count: 1
allele frequency: 8.402090440101497e-6
allele num: 119018
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2824T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3083T>C
  hgvsp: ENSP00000367734.3:p.Ile1028Thr
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3083T>C
  hgvsp: ENSP00000390616.2:p.Ile1028Thr
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3047T>C
  hgvsp: ENSP00000334105.3:p.Ile1016Thr
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2774T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3047T>C
  hgvsp: ENSP00000367762.2:p.Ile1016Thr
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3047T>C
  hgvsp: ENSP00000367754.1:p.Ile1016Thr
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3047T>C
  hgvsp: ENSP00000278655.4:p.Ile1016Thr
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3051+2156T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2738T>C
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4330
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19257
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ile1016Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum

20-9440300-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9440300
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9440300
    reference: chr 20
allele count: 1
allele frequency: 8.370302167908262e-6
allele num: 119470
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2832C>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3051+2164C>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3091C>G
  hgvsp: ENSP00000390616.2:p.Gln1031Glu
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3055C>G
  hgvsp: ENSP00000367762.2:p.Gln1019Glu
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3055C>G
  hgvsp: ENSP00000278655.4:p.Gln1019Glu
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3055C>G
  hgvsp: ENSP00000367754.1:p.Gln1019Glu
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2746C>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2782C>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3091C>G
  hgvsp: ENSP00000367734.3:p.Gln1031Glu
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3055C>G
  hgvsp: ENSP00000334105.3:p.Gln1019Glu
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19647
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32845
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gln1019Glu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

20-9440301-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9440301
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9440301
    reference: chr 20
allele count: 46
allele frequency: 3.848599444463037e-4
allele num: 119524
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3056A>G
  hgvsp: ENSP00000367762.2:p.Gln1019Arg
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3092A>G
  hgvsp: ENSP00000390616.2:p.Gln1031Arg
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3051+2165A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3056A>G
  hgvsp: ENSP00000334105.3:p.Gln1019Arg
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2747A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3056A>G
  hgvsp: ENSP00000278655.4:p.Gln1019Arg
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3092A>G
  hgvsp: ENSP00000367734.3:p.Gln1031Arg
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2833A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2783A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3056A>G
  hgvsp: ENSP00000367754.1:p.Gln1019Arg
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32789
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4383
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 19688
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 47770
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gln1019Arg
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

20-9440311-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9440311
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9440311
    reference: chr 20
allele count: 2
allele frequency: 1.670704201821068e-5
allele num: 119710
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3102G>A
  hgvsp: ENST00000378473.3:c.3102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2757G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3066G>A
  hgvsp: ENST00000278655.4:c.3066G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3066G>A
  hgvsp: ENST00000334005.3:c.3066G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3066G>A
  hgvsp: ENST00000378493.1:c.3066G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3102G>A
  hgvsp: ENST00000414679.2:c.3102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3051+2175G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3066G>A
  hgvsp: ENST00000378501.2:c.3066G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2793G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2843G>A
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4421
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20002
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1201
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Lys1022Lys
num of homozygotes: 1
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

20-9440331-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9440331
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9440331
    reference: chr 20
allele count: 110
allele frequency: 9.191330069018533e-4
allele num: 119678
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3086A>G
  hgvsp: ENSP00000334105.3:p.Asn1029Ser
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3086A>G
  hgvsp: ENSP00000278655.4:p.Asn1029Ser
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2863A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2777A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3086A>G
  hgvsp: ENSP00000367762.2:p.Asn1029Ser
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3122A>G
  hgvsp: ENSP00000390616.2:p.Asn1041Ser
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3122A>G
  hgvsp: ENSP00000367734.3:p.Asn1041Ser
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3051+2195A>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3086A>G
  hgvsp: ENSP00000367754.1:p.Asn1029Ser
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2813A>G
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20065
  bin: 2.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 3.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4365
  bin: 3.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 31023
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1342
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn1029Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

20-9440332-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9440332
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9440332
    reference: chr 20
allele count: 3
allele frequency: 2.507396820620831e-5
allele num: 119646
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2864T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3123T>C
  hgvsp: ENST00000378473.3:c.3123T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3087T>C
  hgvsp: ENST00000378501.2:c.3087T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2778T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2814T>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3087T>C
  hgvsp: ENST00000378493.1:c.3087T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3087T>C
  hgvsp: ENST00000278655.4:c.3087T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3087T>C
  hgvsp: ENST00000334005.3:c.3087T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3123T>C
  hgvsp: ENST00000414679.2:c.3123T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3051+2196T>C
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20113
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30932
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5848
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asn1029Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

20-9440342-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9440342
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9440342
    reference: chr 20
allele count: 2
allele frequency: 1.67372420372571e-5
allele num: 119494
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3133G>T
  hgvsp: ENSP00000367734.3:p.Ala1045Ser
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2874G>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3097G>T
  hgvsp: ENSP00000367762.2:p.Ala1033Ser
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2788G>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3097G>T
  hgvsp: ENSP00000367754.1:p.Ala1033Ser
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2824G>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3097G>T
  hgvsp: ENSP00000278655.4:p.Ala1033Ser
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3133G>T
  hgvsp: ENSP00000390616.2:p.Ala1045Ser
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3051+2206G>T
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3097G>T
  hgvsp: ENSP00000334105.3:p.Ala1033Ser
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4368
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30168
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20059
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 670
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala1033Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

20-9440361-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9440361
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9440361
    reference: chr 20
allele count: 2
allele frequency: 1.679261125104954e-5
allele num: 119100
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2807G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3116G>A
  hgvsp: ENSP00000367762.2:p.Arg1039Gln
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3152G>A
  hgvsp: ENSP00000367734.3:p.Arg1051Gln
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3152G>A
  hgvsp: ENSP00000390616.2:p.Arg1051Gln
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2843G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3116G>A
  hgvsp: ENSP00000367754.1:p.Arg1039Gln
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3116G>A
  hgvsp: ENSP00000278655.4:p.Arg1039Gln
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2893G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3116G>A
  hgvsp: ENSP00000334105.3:p.Arg1039Gln
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3051+2225G>A
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3062
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28736
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4323
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19833
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 969
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg1039Gln
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum

20-9440366-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9440366
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9440366
    reference: chr 20
allele count: 1
allele frequency: 8.40180806909647e-6
allele num: 119022
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3157C>G
  hgvsp: ENSP00000367734.3:p.Leu1053Val
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2898C>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2812C>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3121C>G
  hgvsp: ENSP00000334105.3:p.Leu1041Val
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3121C>G
  hgvsp: ENSP00000367762.2:p.Leu1041Val
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2848C>G
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3121C>G
  hgvsp: ENSP00000278655.4:p.Leu1041Val
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3121C>G
  hgvsp: ENSP00000367754.1:p.Leu1041Val
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3157C>G
  hgvsp: ENSP00000390616.2:p.Leu1053Val
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3051+2230C>G
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19736
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3290
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4282
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu1041Val
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

20-9440392-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9440392
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9440392
    reference: chr 20
allele count: 1
allele frequency: 8.453514125822104e-6
allele num: 118294
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2838G>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3183G>C
  hgvsp: ENST00000378473.3:c.3183G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3147G>C
  hgvsp: ENST00000278655.4:c.3147G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3183G>C
  hgvsp: ENST00000414679.2:c.3183G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2874G>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3147G>C
  hgvsp: ENST00000378493.1:c.3147G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3147G>C
  hgvsp: ENST00000378501.2:c.3147G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2924G>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3051+2256G>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3147G>C
  hgvsp: ENST00000334005.3:c.3147G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3830
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19388
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27771
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5017
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu1049Leu
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

20-9440395-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9440395
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9440395
    reference: chr 20
allele count: 1
allele frequency: 8.458376330079678e-6
allele num: 118226
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3186G>A
  hgvsp: ENST00000414679.2:c.3186G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3150G>A
  hgvsp: ENST00000334005.3:c.3150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2927G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3051+2259G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2841G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3186G>A
  hgvsp: ENST00000378473.3:c.3186G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3150G>A
  hgvsp: ENST00000378493.1:c.3150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3150G>A
  hgvsp: ENST00000278655.4:c.3150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2877G>A
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3150G>A
  hgvsp: ENST00000378501.2:c.3150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3503
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27985
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2603
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4214
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4972
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu1050Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/20-9440396-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9440396
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9440396
    reference: chr 20
allele count: 16
allele frequency: 1.352516526061303e-4
allele num: 118298
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2842A>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000482123
  gene symbol: PLCB4
  hgvsc: ENST00000482123.1:n.2878A>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3151A>C
  hgvsp: ENSP00000367754.1:p.Lys1051Gln
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000492632
  gene symbol: PLCB4
  hgvsc: ENST00000492632.1:n.3051+2260A>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3151A>C
  hgvsp: ENSP00000278655.4:p.Lys1051Gln
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3151A>C
  hgvsp: ENSP00000367762.2:p.Lys1051Gln
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3187A>C
  hgvsp: ENSP00000390616.2:p.Lys1063Gln
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000334105
  ensembl transcript: ENST00000334005
  gene symbol: PLCB4
  hgvsc: ENST00000334005.3:c.3151A>C
  hgvsp: ENSP00000334105.3:p.Lys1051Gln
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000464199
  gene symbol: PLCB4
  hgvsc: ENST00000464199.1:n.2928A>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3187A>C
  hgvsp: ENSP00000367734.3:p.Lys1063Gln
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28212
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2603
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4162
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19486
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 3.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1131
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Lys1051Gln
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/20-9440397-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9440397
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 9440397
    reference: chr 20
allele count: 1
allele frequency: 8.454657670910904e-6
allele num: 118278
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367734
  ensembl transcript: ENST00000378473
  gene symbol: PLCB4
  hgvsc: ENST00000378473.3:c.3188A>C
  hgvsp: ENSP00000367734.3:p.Lys1063Thr
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000390616
  ensembl transcript: ENST00000414679
  gene symbol: PLCB4
  hgvsc: ENST00000414679.2:c.3188A>C
  hgvsp: ENSP00000390616.2:p.Lys1063Thr
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367762
  ensembl transcript: ENST00000378501
  gene symbol: PLCB4
  hgvsc: ENST00000378501.2:c.3152A>C
  hgvsp: ENSP00000367762.2:p.Lys1051Thr
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000367754
  ensembl transcript: ENST00000378493
  gene symbol: PLCB4
  hgvsc: ENST00000378493.1:c.3152A>C
  hgvsp: ENSP00000367754.1:p.Lys1051Thr
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101333
  ensembl transcript: ENST00000473151
  gene symbol: PLCB4
  hgvsc: ENST00000473151.1:n.2843A>C
  variant of: http://identifiers.org/hgnc/9059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101333
  ensembl protein: ENSP00000278655
  ensembl transcript: ENST00000278655
  gene symbol: PLCB4
  hgvsc: ENST00000278655.4:c.3152A>C
  hgvsp: ENSP00000278655.4:p.Lys1051Thr
  variant of: http://identifiers.org/hgnc/9059
canonical: true
consequence: missense
filter: PASS
hgvs: p.Lys1051Thr
num of homozygotes: 0
reference allele: A

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

South Asian
type: Population
allele count: 1
allele frequency: 1.430205949656751e-4
allele num: 6992
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10998
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.8e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.11e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.612e1

FS
type: SiteQuality
SIO_000300: 1.337e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.248e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.65e0

VQSLOD
type: SiteQuality
SIO_000300: -1.484e0

DP
type: SiteQuality
SIO_000300: 4.57802e5

MQRankSum
type: SiteQuality
SIO_000300: -3.27e-1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11010
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7000
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3270
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.21e-1

FS
type: SiteQuality
SIO_000300: 3.68e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.271e1

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

DP
type: SiteQuality
SIO_000300: 4.58592e5

East Asian
type: Population
allele count: 1
allele frequency: 9.345794392523365e-4
allele num: 1070
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3266
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 636
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 212
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.998e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

MQRankSum
type: SiteQuality
SIO_000300: -5.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

DP
type: SiteQuality
SIO_000300: 4.66964e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.68e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.01e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7050
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 270
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 9.012256669069935e-5
allele num: 11096
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.098e0

FS
type: SiteQuality
SIO_000300: 6.532e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

VQSLOD
type: SiteQuality
SIO_000300: -3.402e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.668e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.88e-2

DP
type: SiteQuality
SIO_000300: 4.72848e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.668e0

QD
type: SiteQuality
SIO_000300: 4.75e0

European (Non-Finnish)
type: Population
allele count: 56
allele frequency: 4.983980064079744e-3
allele num: 11236
num of homozygotes: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1094
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 216
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 274
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.459e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.71e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.33e-1

DP
type: SiteQuality
SIO_000300: 4.87521e5

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 276
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3310
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 664
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.13e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.62e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

FS
type: SiteQuality
SIO_000300: 1.519e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.714e1

DP
type: SiteQuality
SIO_000300: 4.9293e5

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 676
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11706
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7272
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.495e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.495e0

MQ
type: SiteQuality
SIO_000300: 6.302e1

MQRankSum
type: SiteQuality
SIO_000300: 1.5e0

QD
type: SiteQuality
SIO_000300: 1.505e1

DP
type: SiteQuality
SIO_000300: 5.06492e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-2

VQSLOD
type: SiteQuality
SIO_000300: -5.9e-2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1188
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 672
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11688
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.73e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.34e-2

DP
type: SiteQuality
SIO_000300: 5.13294e5

QD
type: SiteQuality
SIO_000300: 2.282e1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 304
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11850
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.428571428571429e-3
allele num: 700
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7288
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.428e0

VQSLOD
type: SiteQuality
SIO_000300: -1.098e0

MQRankSum
type: SiteQuality
SIO_000300: 1.93e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.26e-2

QD
type: SiteQuality
SIO_000300: 1.362e1

DP
type: SiteQuality
SIO_000300: 5.24742e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.17e-1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1242
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 314
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 8.378016085790885e-5
allele num: 11936
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.13e-1

QD
type: SiteQuality
SIO_000300: 1.328e1

DP
type: SiteQuality
SIO_000300: 5.32477e5

VQSLOD
type: SiteQuality
SIO_000300: 5.74e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.307e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.59e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 314
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.890173410404624e-4
allele num: 3460
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1242
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 708
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.48e-1

DP
type: SiteQuality
SIO_000300: 5.32477e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

QD
type: SiteQuality
SIO_000300: 1.328e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.307e0

VQSLOD
type: SiteQuality
SIO_000300: 5.74e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.59e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.13e-1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 708
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1242
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 314
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.307e0

VQSLOD
type: SiteQuality
SIO_000300: 5.74e0

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.59e-2

QD
type: SiteQuality
SIO_000300: 1.328e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.48e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.13e-1

DP
type: SiteQuality
SIO_000300: 5.32477e5

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 732
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3486
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 330
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 230
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.11e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

QD
type: SiteQuality
SIO_000300: 8.720000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

FS
type: SiteQuality
SIO_000300: 3.979e0

DP
type: SiteQuality
SIO_000300: 5.39117e5

GenotypeQuality
all individuals: 205
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1638
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1549
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 938
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4220
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10790
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5173
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 781
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32199
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.620640477116556e-5
allele num: 61704
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14018
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7798
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10696
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6448
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9820
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.45e-2

QD
type: SiteQuality
SIO_000300: 1.377e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.81e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.93e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.742e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

DP
type: SiteQuality
SIO_000300: 1.62269e6

GenotypeQuality
all individuals: 55
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1633
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10864
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 788
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 935
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4211
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 415
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32671
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5208
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10712
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9834
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61736
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6452
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.563445270443476e-4
allele num: 7802
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14054
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.13e-1

DP
type: SiteQuality
SIO_000300: 1.621102e6

VQSLOD
type: SiteQuality
SIO_000300: -8.791e-1

FS
type: SiteQuality
SIO_000300: 1.433e0

QD
type: SiteQuality
SIO_000300: 5.89e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.16e-1

MQ
type: SiteQuality
SIO_000300: 5.906e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e-1

GenotypeQuality
all individuals: 4212
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 4771
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29803
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13031
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1993
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2100
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 740
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9730
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7594
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13728
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.923521302435502e-5
allele num: 60932
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.532888465204957e-5
allele num: 10490
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.865e1

FS
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SIO_000300: 0.0e0

DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -6.337e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.080000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 1.416831963729102e-4
allele num: 7058
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6252
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 58188
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 9938
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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VQSLOD
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MQ
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MQRankSum
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QD
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InbreedingCoeff
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SIO_000300: -2.6e-3

DP
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SIO_000300: 1.387656e6

ClippingRankSum
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SIO_000300: -1.401e0

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

European (Non-Finnish)
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allele frequency: 1.802711277761754e-5
allele num: 55472
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9442
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9072
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6132
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 742
num of homozygotes: 0

South Asian
type: Population
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allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.82e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.15e0

MQRankSum
type: SiteQuality
SIO_000300: 9.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

MQ
type: SiteQuality
SIO_000300: 5.961e1

ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.893e0

DP
type: SiteQuality
SIO_000300: 1.212339e6

QD
type: SiteQuality
SIO_000300: 1.512e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5816
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52240
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 708
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.398496240601504e-5
allele num: 10640
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8870
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5978
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.43e-1

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

DP
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SIO_000300: 1.124406e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.106e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.53e0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5820
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.020365282042993e-5
allele num: 49496
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 664
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5300
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9768
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.66e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.10278e6

QD
type: SiteQuality
SIO_000300: 9.789999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

VQSLOD
type: SiteQuality
SIO_000300: 2.62e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: 4.66e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
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num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.537799101925324e-5
allele num: 65028
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 2.5e-3

DP
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QD
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
type: SiteQuality
SIO_000300: -8.1e-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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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
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allele num: 65148
num of homozygotes: 0

Latino
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Other
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East Asian
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African
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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MQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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FS
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DP
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InbreedingCoeff
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QD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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allele num: 11320
num of homozygotes: 0

East Asian
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allele frequency: 2.36707938820102e-2
allele num: 8238
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European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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allele frequency: 1.131221719457014e-3
allele num: 884
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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VQSLOD
type: SiteQuality
SIO_000300: 5.91e0

BaseQRankSum
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InbreedingCoeff
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SIO_000300: 2.0e-2

MQ
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FS
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QD
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ReadPosRankSum
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DP
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MQRankSum
type: SiteQuality
SIO_000300: 1.83e-1

ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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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
allele num: 65208
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East Asian
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South Asian
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allele frequency: 6.140997297961189e-5
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BaseQRankSum
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MQRankSum
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MQ
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FS
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DP
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ClippingRankSum
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SIO_000300: -5.91e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.25e-1

QD
type: SiteQuality
SIO_000300: 1.411e1

VQSLOD
type: SiteQuality
SIO_000300: 5.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11340
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16292
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8276
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.530221882172915e-5
allele num: 65350
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.31e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.611e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

DP
type: SiteQuality
SIO_000300: 1.825387e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.54e0

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 3.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.225e0

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

South Asian
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allele frequency: 0.0e0
allele num: 16324
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8358
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.791981712678038e-5
allele num: 11374
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9844
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65616
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.162e1

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.843476e6

MQRankSum
type: SiteQuality
SIO_000300: 8.120000000000001e-1

FS
type: SiteQuality
SIO_000300: 1.159e0

VQSLOD
type: SiteQuality
SIO_000300: 9.57e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.48e-1

MQ
type: SiteQuality
SIO_000300: 5.945e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.252e0

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

GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65784
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11394
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.011122345803842e-4
allele num: 9890
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.41e0

QD
type: SiteQuality
SIO_000300: 8.27e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.8e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.88e-1

DP
type: SiteQuality
SIO_000300: 1.853618e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.38e-1

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
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: 8484
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.095330976472023e-5
allele num: 16406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66058
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9948
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.43e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.15e0

MQRankSum
type: SiteQuality
SIO_000300: -2.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.97e-1

FS
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.7e-1

QD
type: SiteQuality
SIO_000300: 1.379e1

DP
type: SiteQuality
SIO_000300: 1.86512e6

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 204
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 2.625590757920532e-4
allele num: 11426
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9984
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
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: 8500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66124
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.666e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.219e0

DP
type: SiteQuality
SIO_000300: 1.867576e6

MQ
type: SiteQuality
SIO_000300: 5.948e1

MQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

QD
type: SiteQuality
SIO_000300: 1.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.57e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.929e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 132

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 113
allele frequency: 1.708290500090706e-3
allele num: 66148
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 12
allele frequency: 1.820388349514563e-3
allele num: 6592
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16422
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 5.007009813739235e-4
allele num: 9986
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.11358574610245e-3
allele num: 898
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.749475157452764e-4
allele num: 11432
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.51e0

FS
type: SiteQuality
SIO_000300: 6.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.35e-1

QD
type: SiteQuality
SIO_000300: 1.475e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

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

DP
type: SiteQuality
SIO_000300: 1.871582e6

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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.215657670799903e-4
allele num: 16452
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.01295570955107e-5
allele num: 66380
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
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allele num: 10122
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e-1

DP
type: SiteQuality
SIO_000300: 1.878642e6

MQRankSum
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.811e0

InbreedingCoeff
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.4e-1

QD
type: SiteQuality
SIO_000300: 9.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.39e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9902
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variant carriers: 11

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

Other
type: Population
allele count: 1
allele frequency: 1.11358574610245e-3
allele num: 898
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 4.861448711716091e-4
allele num: 16456
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506387081224391e-5
allele num: 66384
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.877518767285657e-5
allele num: 10124
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.448e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.649999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.44e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.153e1

DP
type: SiteQuality
SIO_000300: 1.879488e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.957e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.14e-1

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26219
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7736
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9892
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 64
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3262
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3752
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4701
bin: 7.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.873617693522907e-5
allele num: 10128
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66412
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.109e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.880242e6

MQRankSum
type: SiteQuality
SIO_000300: 6.33e-1

QD
type: SiteQuality
SIO_000300: 8.789999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.32e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.269e0

VQSLOD
type: SiteQuality
SIO_000300: 4.64e0

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4705
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3262
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3754
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7737
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9891
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2374
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 2.75e1
variant carriers: 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: 898
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10140
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505434618974498e-5
allele num: 66426
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 7.37e0

FS
type: SiteQuality
SIO_000300: 3.78e0

DP
type: SiteQuality
SIO_000300: 1.880496e6

VQSLOD
type: SiteQuality
SIO_000300: -1.188e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.64e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.83e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeQuality
all individuals: 3734
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 91
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 78
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 418
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 3241
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variant carriers: 0

GenotypeQuality
all individuals: 2366
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26300
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7715
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variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4683
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10080
bin: 9.75e1
variant carriers: 209

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

GenotypeQuality
all individuals: 1694
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66456
num of homozygotes: 0

South Asian
type: Population
allele count: 210
allele frequency: 1.275355277541601e-2
allele num: 16466
num of homozygotes: 3

Other
type: Population
allele count: 1
allele frequency: 1.11358574610245e-3
allele num: 898
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.832841691248771e-5
allele num: 10170
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.23e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.27e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.5e0

DP
type: SiteQuality
SIO_000300: 1.890199e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.05e-2

QD
type: SiteQuality
SIO_000300: 1.206e1

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

GenotypeQuality
all individuals: 422
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1696
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26405
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3745
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7750
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 90
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3259
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9897
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 60
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2371
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4705
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 2.610057421263268e-4
allele num: 11494
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: 66450
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 2.93e0

QD
type: SiteQuality
SIO_000300: 1.734e1

MQ
type: SiteQuality
SIO_000300: 6.141e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.51e-1

DP
type: SiteQuality
SIO_000300: 1.882827e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.034e0

MQRankSum
type: SiteQuality
SIO_000300: 2.67e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.81e-1

GenotypeQuality
all individuals: 13
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26447
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variant carriers: 0

GenotypeQuality
all individuals: 7763
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variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3745
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 53
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variant carriers: 0

GenotypeQuality
all individuals: 3262
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9895
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4702
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2372
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504573904670197e-5
allele num: 66464
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
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: 16464
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.963e1

VQSLOD
type: SiteQuality
SIO_000300: 3.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.29e0

DP
type: SiteQuality
SIO_000300: 1.883192e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

FS
type: SiteQuality
SIO_000300: 9.727e0

MQRankSum
type: SiteQuality
SIO_000300: -7.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.192e0

QD
type: SiteQuality
SIO_000300: 1.433e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
all individuals: 3745
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4701
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 409
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variant carriers: 0

GenotypeQuality
all individuals: 2370
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variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
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variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

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

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 55
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variant carriers: 0

GenotypeQuality
all individuals: 76
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26413
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7762
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.0530749789385e-4
allele num: 66472
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10182
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.70170553428472e-5
allele num: 11492
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.419e0

VQSLOD
type: SiteQuality
SIO_000300: 6.909999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.945e1

FS
type: SiteQuality
SIO_000300: 3.238e0

QD
type: SiteQuality
SIO_000300: 1.043e1

DP
type: SiteQuality
SIO_000300: 1.883783e6

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.39e-1

GenotypeQuality
all individuals: 400
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 26208
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variant carriers: 2

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 79
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variant carriers: 0

GenotypeQuality
all individuals: 76
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GenotypeQuality
all individuals: 3216
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variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4642
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 47
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3700
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 61
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2329
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1659
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10451
bin: 9.75e1
variant carriers: 776

GenotypeQuality
all individuals: 7707
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.821714840903571e-4
allele num: 16468
num of homozygotes: 0

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

Latino
type: Population
allele count: 39
allele frequency: 3.392484342379958e-3
allele num: 11496
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 1.955298859910357e-4
allele num: 66486
num of homozygotes: 0

African
type: Population
allele count: 767
allele frequency: 7.510771641206423e-2
allele num: 10212
num of homozygotes: 33

Other
type: Population
allele count: 2
allele frequency: 2.2271714922049e-3
allele num: 898
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.75e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.88e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.46e-1

QD
type: SiteQuality
SIO_000300: 1.311e1

MQRankSum
type: SiteQuality
SIO_000300: 2.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.205e0

DP
type: SiteQuality
SIO_000300: 1.916238e6

GenotypeQuality
all individuals: 48
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7796
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9864
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 35
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variant carriers: 0

GenotypeQuality
all individuals: 415
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variant carriers: 0

GenotypeQuality
all individuals: 3253
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variant carriers: 0

GenotypeQuality
all individuals: 26430
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3750
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 1686
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variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2366
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4693
bin: 7.75e1
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
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East Asian
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allele frequency: 1.162250116225012e-4
allele num: 8604
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European (Non-Finnish)
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allele count: 7
allele frequency: 1.052853232259423e-4
allele num: 66486
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10206
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6604
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South Asian
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allele frequency: 6.072382803011902e-5
allele num: 16468
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MQRankSum
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SIO_000300: -5.8e-2

VQSLOD
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DP
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SIO_000300: 1.886071e6

ReadPosRankSum
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SIO_000300: 7.71e-1

BaseQRankSum
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SIO_000300: 1.49e-1

ClippingRankSum
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SIO_000300: -7.83e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
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SIO_000300: 5.955e1

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

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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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 10206
num of homozygotes: 0

East Asian
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allele frequency: 2.324500232450023e-4
allele num: 8604
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.504166541319455e-5
allele num: 66482
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6604
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South Asian
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allele frequency: 6.073120369245719e-5
allele num: 16466
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Latino
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allele frequency: 0.0e0
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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QD
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BaseQRankSum
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FS
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MQ
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DP
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ClippingRankSum
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SIO_000300: 2.3e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

East Asian
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allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66494
num of homozygotes: 0

African
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allele count: 2
allele frequency: 1.958863858961802e-4
allele num: 10210
num of homozygotes: 0

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

South Asian
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allele count: 3
allele frequency: 1.822157434402332e-4
allele num: 16464
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
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SIO_000300: 1.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-2

BaseQRankSum
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QD
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VQSLOD
type: SiteQuality
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MQ
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FS
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SIO_000300: 1.159e0

DP
type: SiteQuality
SIO_000300: 1.885955e6

ReadPosRankSum
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SIO_000300: -3.87e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16470
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: 8608
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.796238244514106e-5
allele num: 10208
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66488
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.885447e6

VQSLOD
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QD
type: SiteQuality
SIO_000300: 1.49e1

BaseQRankSum
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SIO_000300: -2.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.899e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.74e0

ReadPosRankSum
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SIO_000300: -1.606e0

FS
type: SiteQuality
SIO_000300: 5.051e0

MQRankSum
type: SiteQuality
SIO_000300: 2.4e-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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GenotypeQuality
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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: 4

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.514129224472599e-5
allele num: 66458
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 1.515151515151515e-4
allele num: 6600
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16458
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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InbreedingCoeff
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QD
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VQSLOD
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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SIO_000300: 4.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.89e-1

DP
type: SiteQuality
SIO_000300: 1.88375e6

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

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

European (Finnish)
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allele count: 0
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East Asian
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South Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 9.823182711198428e-5
allele num: 10180
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e-1

DP
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ReadPosRankSum
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FS
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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MQRankSum
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MQ
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QD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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European (Finnish)
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South Asian
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Latino
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East Asian
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Other
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ReadPosRankSum
type: SiteQuality
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FS
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DP
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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QD
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MQRankSum
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MQ
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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allele num: 66330
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European (Finnish)
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African
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allele frequency: 1.816745655608215e-2
allele num: 10128
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Latino
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allele frequency: 9.576876197109525e-4
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South Asian
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Other
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DP
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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QD
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FS
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InbreedingCoeff
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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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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22003
bin: 6.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16420
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508750754375377e-5
allele num: 66280
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: 8534
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.463e1

MQRankSum
type: SiteQuality
SIO_000300: -1.51e-1

DP
type: SiteQuality
SIO_000300: 1.852364e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.27e-1

MQ
type: SiteQuality
SIO_000300: 5.822e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.62e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.43e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.506e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

GenotypeQuality
all individuals: 48
bin: 1.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1413
bin: 2.25e1
variant carriers: 9

GenotypeQuality
all individuals: 58
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 17582
bin: 9.75e1
variant carriers: 10244

GenotypeQuality
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bin: 3.25e1
variant carriers: 6

GenotypeQuality
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bin: 4.75e1
variant carriers: 9

GenotypeQuality
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bin: 4.25e1
variant carriers: 7

GenotypeQuality
all individuals: 2940
bin: 8.25e1
variant carriers: 21

GenotypeQuality
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bin: 8.75e1
variant carriers: 22

GenotypeQuality
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bin: 9.25e1
variant carriers: 23

GenotypeQuality
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bin: 5.25e1
variant carriers: 9

GenotypeQuality
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variant carriers: 13

GenotypeQuality
all individuals: 6205
bin: 6.75e1
variant carriers: 31

GenotypeQuality
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variant carriers: 10

GenotypeQuality
all individuals: 18340
bin: 6.25e1
variant carriers: 19

GenotypeQuality
all individuals: 3748
bin: 7.75e1
variant carriers: 29

Latino
type: Population
allele count: 1300
allele frequency: 1.136165006117812e-1
allele num: 11442
num of homozygotes: 77

Other
type: Population
allele count: 75
allele frequency: 8.370535714285714e-2
allele num: 896
num of homozygotes: 4

South Asian
type: Population
allele count: 517
allele frequency: 3.149750213232606e-2
allele num: 16414
num of homozygotes: 14

African
type: Population
allele count: 1335
allele frequency: 1.324404761904762e-1
allele num: 10080
num of homozygotes: 87

East Asian
type: Population
allele count: 547
allele frequency: 6.417175035194744e-2
allele num: 8524
num of homozygotes: 20

European (Non-Finnish)
type: Population
allele count: 6831
allele frequency: 1.032216144337997e-1
allele num: 66178
num of homozygotes: 353

European (Finnish)
type: Population
allele count: 402
allele frequency: 6.10200364298725e-2
allele num: 6588
num of homozygotes: 13

QD
type: SiteQuality
SIO_000300: 1.614e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.12e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.6e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.1e-2

DP
type: SiteQuality
SIO_000300: 1.983745e6

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.76e-1

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2050
bin: 3.25e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9547
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1133
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8490
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10002
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16392
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.537342327354124e-5
allele num: 66118
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.32e-1

FS
type: SiteQuality
SIO_000300: 1.28e0

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.46e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.83e-1

DP
type: SiteQuality
SIO_000300: 1.841545e6

GenotypeQuality
all individuals: 154
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 739
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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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 289
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variant carriers: 0

GenotypeQuality
all individuals: 9543
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9992
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8474
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16390
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11434
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513179796023364e-5
allele num: 66086
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.878e0

DP
type: SiteQuality
SIO_000300: 1.83872e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.347e0

MQRankSum
type: SiteQuality
SIO_000300: -1.506e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.927e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.25e0

GenotypeQuality
all individuals: 1586
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2524
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6411
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1545
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variant carriers: 0

GenotypeQuality
all individuals: 1046
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variant carriers: 0

GenotypeQuality
all individuals: 2188
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variant carriers: 0

GenotypeQuality
all individuals: 30
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GenotypeQuality
all individuals: 265
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 473
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GenotypeQuality
all individuals: 1716
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9542
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variant carriers: 1

GenotypeQuality
all individuals: 3566
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2962
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13423
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518095700752976e-5
allele num: 65872
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9932
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8418
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16372
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.418e0

MQ
type: SiteQuality
SIO_000300: 5.695e1

DP
type: SiteQuality
SIO_000300: 1.827514e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.485e0

QD
type: SiteQuality
SIO_000300: 6.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.388e0

MQRankSum
type: SiteQuality
SIO_000300: -4.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.39e-1

GenotypeQuality
all individuals: 217
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2094
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variant carriers: 0

GenotypeQuality
all individuals: 1753
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GenotypeQuality
all individuals: 760
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variant carriers: 0

GenotypeQuality
all individuals: 680
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GenotypeQuality
all individuals: 57
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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: 4775
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 991
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variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12296
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63362
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11104
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: 0
allele frequency: 0.0e0
allele num: 8312
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.03950103950104e-4
allele num: 9620
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.95e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.892e-1

MQ
type: SiteQuality
SIO_000300: 5.875e1

DP
type: SiteQuality
SIO_000300: 1.288948e6

FS
type: SiteQuality
SIO_000300: 3.121e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.94e-1

QD
type: SiteQuality
SIO_000300: 1.335e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

GenotypeQuality
all individuals: 1690
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3147
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GenotypeQuality
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GenotypeQuality
all individuals: 216
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GenotypeQuality
all individuals: 679
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GenotypeQuality
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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: 323
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12344
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9636
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6474
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: 0
allele frequency: 0.0e0
allele num: 8308
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11104
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.579329732461543e-5
allele num: 63318
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.114e1

FS
type: SiteQuality
SIO_000300: 1.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.54e0

DP
type: SiteQuality
SIO_000300: 1.300341e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.0e-2

GenotypeQuality
all individuals: 372
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
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variant carriers: 0

GenotypeQuality
all individuals: 48
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GenotypeQuality
all individuals: 40676
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 684
bin: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12812
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8402
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63846
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11162
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.054653790836244e-4
allele num: 9734
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 7.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.74e-1

FS
type: SiteQuality
SIO_000300: 1.773e0

MQRankSum
type: SiteQuality
SIO_000300: 8.79e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.363578e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

QD
type: SiteQuality
SIO_000300: 1.435e1

VQSLOD
type: SiteQuality
SIO_000300: 1.36e0

GenotypeQuality
all individuals: 57
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 8.25e1
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GenotypeQuality
all individuals: 73
bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 434
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GenotypeQuality
all individuals: 132
bin: 9.25e1
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GenotypeQuality
all individuals: 90
bin: 1.75e1
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GenotypeQuality
all individuals: 277
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5342
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13158
num of homozygotes: 0

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

African
type: Population
allele count: 3
allele frequency: 3.068112088361628e-4
allele num: 9778
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64118
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11216
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8418
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6500
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.834e1

FS
type: SiteQuality
SIO_000300: 5.703e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e-1

QD
type: SiteQuality
SIO_000300: 1.437e1

DP
type: SiteQuality
SIO_000300: 1.384257e6

VQSLOD
type: SiteQuality
SIO_000300: -7.365e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.81e-1

GenotypeQuality
all individuals: 399
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 938
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 63
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variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.372479240806643e-4
allele num: 8430
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.914244963451596e-5
allele num: 11218
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.225099601593625e-5
allele num: 64256
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13432
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6498
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.239e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

FS
type: SiteQuality
SIO_000300: 6.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.66e0

DP
type: SiteQuality
SIO_000300: 1.392763e6

MQRankSum
type: SiteQuality
SIO_000300: 7.05e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

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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bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65024
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.854258898530193e-5
allele num: 11294
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14506
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.17e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.3e0

QD
type: SiteQuality
SIO_000300: 1.117e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.999999999999999e-3

DP
type: SiteQuality
SIO_000300: 1.433359e6

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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GenotypeQuality
all individuals: 136
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variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519202722411279e-5
allele num: 65824
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8528
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10072
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11384
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15756
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 8.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

FS
type: SiteQuality
SIO_000300: 2.316e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.95e0

MQRankSum
type: SiteQuality
SIO_000300: 6.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.56e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.471312e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.62e-1

GenotypeQuality
all individuals: 204
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variant carriers: 0

GenotypeQuality
all individuals: 291
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GenotypeQuality
all individuals: 16
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 471
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GenotypeQuality
all individuals: 679
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variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16012
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515610791148833e-5
allele num: 65980
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10098
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11392
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.73e-1

FS
type: SiteQuality
SIO_000300: 5.03e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.677e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.8e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -3.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.33e-1

DP
type: SiteQuality
SIO_000300: 1.478705e6

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
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variant carriers: 0

GenotypeQuality
all individuals: 20
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 474
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10104
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.131221719457014e-3
allele num: 884
num of homozygotes: 0

South Asian
type: Population
allele count: 39
allele frequency: 2.432331295996008e-3
allele num: 16034
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.575757575757576e-5
allele num: 66000
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.775008775008775e-5
allele num: 11396
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.479015e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.52e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.32e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.837e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.42e-1

QD
type: SiteQuality
SIO_000300: 1.156e1

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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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 2
allele frequency: 1.239157372986369e-4
allele num: 16140
num of homozygotes: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66068
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10126
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8526
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.038e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.69e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.11e-2

DP
type: SiteQuality
SIO_000300: 1.48087e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.503e0

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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variant carriers: 110

GenotypeQuality
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GenotypeQuality
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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: 128
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11366
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10102
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66048
num of homozygotes: 0

East Asian
type: Population
allele count: 109
allele frequency: 1.27724396531521e-2
allele num: 8534
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.181233774261343e-5
allele num: 16178
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.27e-1

DP
type: SiteQuality
SIO_000300: 1.475462e6

FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
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VQSLOD
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InbreedingCoeff
type: SiteQuality
SIO_000300: 9.7e-3

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.37e0

GenotypeQuality
all individuals: 46087
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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
all individuals: 1527
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GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.543526988550312e-5
allele num: 66028
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10098
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11358
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16174
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.473352e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

QD
type: SiteQuality
SIO_000300: 1.217e1

FS
type: SiteQuality
SIO_000300: 2.4e0

MQRankSum
type: SiteQuality
SIO_000300: 1.68e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.73e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-2

GenotypeQuality
all individuals: 376
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45007
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1280
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5718
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 767
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1730
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1056
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 705
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 763
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8520
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11338
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16168
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.031772980839195e-5
allele num: 65968
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.127e1

MQRankSum
type: SiteQuality
SIO_000300: 6.31e-1

DP
type: SiteQuality
SIO_000300: 1.468107e6

MQ
type: SiteQuality
SIO_000300: 5.954e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.12e-1

FS
type: SiteQuality
SIO_000300: 1.422e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.718e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.88e-1

GenotypeQuality
all individuals: 1111
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5469
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1110
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 860
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 624
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2246
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1212
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43347
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1019
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 920
bin: 5.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16090
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519664458087654e-5
allele num: 65804
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.00080064051241e-4
allele num: 9992
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11298
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.826e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.454876e6

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

FS
type: SiteQuality
SIO_000300: 5.802e0

QD
type: SiteQuality
SIO_000300: 1.444e1

MQRankSum
type: SiteQuality
SIO_000300: 4.62e-1

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 886
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 991
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5452
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 851
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 638
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2389
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1014
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1195
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43065
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1163
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1186
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.225874735400324e-5
allele num: 16062
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11290
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65782
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 6.46e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

QD
type: SiteQuality
SIO_000300: 1.243e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.375e0

MQ
type: SiteQuality
SIO_000300: 5.934e1

FS
type: SiteQuality
SIO_000300: 3.817e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.562e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e0

DP
type: SiteQuality
SIO_000300: 1.450986e6

GenotypeQuality
all individuals: 97
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1405
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1295
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1463
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 982
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1250
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2921
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41134
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1078
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1070
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 879
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 792
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.911067545891998e-5
allele num: 11222
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9912
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15862
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65442
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6498
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.23e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -6.776e-1

DP
type: SiteQuality
SIO_000300: 1.438072e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

FS
type: SiteQuality
SIO_000300: 4.467e0

QD
type: SiteQuality
SIO_000300: 8.720000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.905e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.482e0

GenotypeQuality
all individuals: 27
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1219
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 728
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2918
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 862
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variant carriers: 0

GenotypeQuality
all individuals: 1160
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
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variant carriers: 0

GenotypeQuality
all individuals: 63
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variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 42622
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variant carriers: 0

GenotypeQuality
all individuals: 927
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variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1070
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1243
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1049
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65414
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.310740880979428e-5
allele num: 15846
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.399999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.07e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.88e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.693e0

DP
type: SiteQuality
SIO_000300: 1.441201e6

MQ
type: SiteQuality
SIO_000300: 5.851e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.165e0

QD
type: SiteQuality
SIO_000300: 7.71e0

GenotypeQuality
all individuals: 43279
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2921
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 893
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
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variant carriers: 0

GenotypeQuality
all individuals: 861
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 894
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1051
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1141
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5016
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1124
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 672
bin: 9.75e1
variant carriers: 16

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

African
type: Population
allele count: 16
allele frequency: 1.612578109252167e-3
allele num: 9922
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65456
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6496
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15836
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8478
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.292e1

FS
type: SiteQuality
SIO_000300: 2.452e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.16e0

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e-1

DP
type: SiteQuality
SIO_000300: 1.441151e6

MQRankSum
type: SiteQuality
SIO_000300: -6.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e-1