12-133196381-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196381
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196381
    reference: chr 12
allele count: 2
allele frequency: 1.971608832807571e-5
allele num: 101440
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.381+45G>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.310-49G>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.381+45G>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.106-49G>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.338+45G>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.413+45G>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.310-49G>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.381+45G>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-205G>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.248+45G>T
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6928
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12672
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16002
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10551
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8805
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 596
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3628
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3332
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

12-133196398-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196398
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196398
    reference: chr 12
allele count: 1
allele frequency: 9.979641531276197e-6
allele num: 100204
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.310-32C>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.106-32C>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.310-32C>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.382-32C>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.382-32C>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-188C>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.339-32C>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.414-32C>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.249-32C>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.382-32C>G
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9802
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7349
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2493
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16457
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10934
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1620
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 887
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2149
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

12-133196399-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196399
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196399
    reference: chr 12
allele count: 1
allele frequency: 9.956192751891677e-6
allele num: 100440
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.310-31G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.339-31G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.310-31G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.249-31G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.382-31G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.382-31G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.382-31G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-187G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.106-31G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.414-31G>A
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2468
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10940
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10724
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7385
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16764
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9505
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 674
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1587
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2013
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3890
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

12-133196400-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196400
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196400
    reference: chr 12
allele count: 1
allele frequency: 9.934827531394055e-6
allele num: 100656
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.414-30G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.382-30G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.382-30G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.382-30G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-186G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.310-30G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.106-30G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.339-30G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.310-30G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.249-30G>A
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9504
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10678
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10941
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7437
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21906
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11852
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2445
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

12-133196406-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196406
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196406
    reference: chr 12
allele count: 2
allele frequency: 1.993024414549078e-5
allele num: 100350
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.382-24C>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.382-24C>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.106-24C>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.249-24C>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.310-24C>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.382-24C>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.339-24C>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.310-24C>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.414-24C>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-180C>G
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2422
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10874
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16901
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10436
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7489
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9683
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2253
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3882
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11466
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/12-133196409-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196409
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196409
    reference: chr 12
allele count: 1
allele frequency: 9.945894334818586e-6
allele num: 100544
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-177A>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.249-21A>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.414-21A>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.339-21A>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.310-21A>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.106-21A>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.382-21A>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.382-21A>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.310-21A>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.382-21A>C
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10757
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10412
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7541
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3514
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3827
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD

12-133196414-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196414
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196414
    reference: chr 12
allele count: 1
allele frequency: 9.959167413604222e-6
allele num: 100410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.382-16G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.382-16G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.414-16G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.339-16G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.249-16G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.310-16G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-172G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.382-16G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.310-16G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.106-16G>A
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10331
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7524
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8769
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18435
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22998
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 700
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11418
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

12-133196416-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196416
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196416
    reference: chr 12
allele count: 56
allele frequency: 5.564277339480534e-4
allele num: 100642
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.414-14C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.382-14C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.382-14C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.106-14C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.310-14C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.310-14C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.382-14C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-170C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.339-14C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.249-14C>T
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18728
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7502
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8577
  bin: 1.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 10373
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10281
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 741
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 9.25e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum

12-133196418-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196418
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196418
    reference: chr 12
allele count: 2
allele frequency: 1.983615337313788e-5
allele num: 100826
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.249-12C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.310-12C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.382-12C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.382-12C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.106-12C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.339-12C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-168C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.310-12C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.382-12C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.414-12C>T
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7484
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7974
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10531
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2348
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19494
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10026
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1726
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

12-133196425-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196425
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196425
    reference: chr 12
allele count: 3
allele frequency: 2.961851354553353e-5
allele num: 101288
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.382-5C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.310-5C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.249-5C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.106-5C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.382-5C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.339-5C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.414-5C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.382-5C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.310-5C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-161C>T
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6308
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11173
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7360
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21587
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 777
  bin: 7.75e1
  variant carriers: 0
hgvs: c.382-5C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

12-133196435-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196435
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196435
    reference: chr 12
allele count: 1
allele frequency: 9.828396202307707e-6
allele num: 101746
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.254A>G
  hgvsp: ENSP00000437646.1:p.Ile85Met
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.387A>G
  hgvsp: ENSP00000373762.3:p.Ile129Met
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.315A>G
  hgvsp: ENSP00000405531.2:p.Ile105Met
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.315A>G
  hgvsp: ENSP00000343904.5:p.Ile105Met
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.344A>G
  hgvsp: ENSP00000444853.1:p.Ile115Met
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.387A>G
  hgvsp: ENSP00000343339.4:p.Ile129Met
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.419A>G
  hgvsp: ENSP00000444477.1:p.Ile140Met
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.111A>G
  hgvsp: ENSP00000344502.4:p.Ile37Met
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-151A>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.387A>G
  hgvsp: ENSP00000345095.5:p.Ile129Met
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8062
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2296
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11406
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23652
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7262
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1932
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile129Met
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

12-133196438-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196438
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196438
    reference: chr 12
allele count: 1
allele frequency: 9.819324430479183e-6
allele num: 101840
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.114G>T
  hgvsp: ENSP00000344502.4:p.Arg38Ser
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.318G>T
  hgvsp: ENSP00000343904.5:p.Arg106Ser
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.390G>T
  hgvsp: ENSP00000373762.3:p.Arg130Ser
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.390G>T
  hgvsp: ENSP00000343339.4:p.Arg130Ser
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.390G>T
  hgvsp: ENSP00000345095.5:p.Arg130Ser
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.422G>T
  hgvsp: ENSP00000444477.1:p.Arg141Ser
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.318G>T
  hgvsp: ENSP00000405531.2:p.Arg106Ser
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.347G>T
  hgvsp: ENSP00000444853.1:p.Arg116Ser
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.257G>T
  hgvsp: ENSP00000437646.1:p.Arg86Ser
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-148G>T
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4907
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11567
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7689
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9829
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg130Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

12-133196440-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196440
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196440
    reference: chr 12
allele count: 1
allele frequency: 9.831681610822715e-6
allele num: 101712
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.392T>C
  hgvsp: ENSP00000343339.4:p.Val131Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.349T>C
  hgvsp: ENSP00000444853.1:p.Val117Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.116T>C
  hgvsp: ENSP00000344502.4:p.Val39Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.259T>C
  hgvsp: ENSP00000437646.1:p.Val87Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.320T>C
  hgvsp: ENSP00000405531.2:p.Val107Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.392T>C
  hgvsp: ENSP00000373762.3:p.Val131Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.424T>C
  hgvsp: ENSP00000444477.1:p.Val142Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.392T>C
  hgvsp: ENSP00000345095.5:p.Val131Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.320T>C
  hgvsp: ENSP00000343904.5:p.Val107Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-146T>C
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7150
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7615
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24202
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4916
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11660
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val131Ala
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/12-133196444-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196444
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196444
    reference: chr 12
allele count: 1
allele frequency: 9.811616954474098e-6
allele num: 101920
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.396C>A
  hgvsp: ENSP00000345095.5:p.His132Gln
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.428C>A
  hgvsp: ENSP00000444477.1:p.His143Gln
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.120C>A
  hgvsp: ENSP00000344502.4:p.His40Gln
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.324C>A
  hgvsp: ENSP00000343904.5:p.His108Gln
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.396C>A
  hgvsp: ENSP00000343339.4:p.His132Gln
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.263C>A
  hgvsp: ENSP00000437646.1:p.His88Gln
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.353C>A
  hgvsp: ENSP00000444853.1:p.His118Gln
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.396C>A
  hgvsp: ENSP00000373762.3:p.His132Gln
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-142C>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.324C>A
  hgvsp: ENSP00000405531.2:p.His108Gln
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4674
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7362
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11794
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4087
  bin: 6.75e1
  variant carriers: 0
hgvs: p.His132Gln
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

12-133196445-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196445
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196445
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 102038
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.121A>G
  hgvsp: ENSP00000344502.4:p.Asn41Asp
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.325A>G
  hgvsp: ENSP00000405531.2:p.Asn109Asp
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.264A>G
  hgvsp: ENSP00000437646.1:p.Asn89Asp
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.354A>G
  hgvsp: ENSP00000444853.1:p.Asn119Asp
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.397A>G
  hgvsp: ENSP00000343339.4:p.Asn133Asp
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.429A>G
  hgvsp: ENSP00000444477.1:p.Asn144Asp
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.397A>G
  hgvsp: ENSP00000345095.5:p.Asn133Asp
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-141A>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.397A>G
  hgvsp: ENSP00000373762.3:p.Asn133Asp
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.325A>G
  hgvsp: ENSP00000343904.5:p.Asn109Asp
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7131
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11787
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24701
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7321
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4598
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 9.75e1
  variant carriers: 0
hgvs: p.Asn133Asp
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/12-133196446-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196446
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196446
    reference: chr 12
allele count: 1
allele frequency: 9.820867379006914e-6
allele num: 101824
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.326A>C
  hgvsp: ENSP00000343904.5:p.Asn109Thr
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.355A>C
  hgvsp: ENSP00000444853.1:p.Asn119Thr
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-140A>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.398A>C
  hgvsp: ENSP00000373762.3:p.Asn133Thr
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.326A>C
  hgvsp: ENSP00000405531.2:p.Asn109Thr
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.430A>C
  hgvsp: ENSP00000444477.1:p.Asn144Thr
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.398A>C
  hgvsp: ENSP00000345095.5:p.Asn133Thr
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.398A>C
  hgvsp: ENSP00000343339.4:p.Asn133Thr
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.122A>C
  hgvsp: ENSP00000344502.4:p.Asn41Thr
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.265A>C
  hgvsp: ENSP00000437646.1:p.Asn89Thr
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4814
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24482
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn133Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

12-133196446-ACGC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196446
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196443
    reference: chr 12
allele count: 1
allele frequency: 9.820867379006914e-6
allele num: 101824
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.328_330delGCC
  hgvsp: ENSP00000343904.5:p.Ala110del
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.432_434delGCC
  hgvsp: ENSP00000444477.1:p.Ala145del
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.267_269delGCC
  hgvsp: ENSP00000437646.1:p.Ala90del
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.124_126delGCC
  hgvsp: ENSP00000344502.4:p.Ala42del
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.400_402delGCC
  hgvsp: ENSP00000345095.5:p.Ala134del
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.328_330delGCC
  hgvsp: ENSP00000405531.2:p.Ala110del
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-138_242-136delGCC
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.400_402delGCC
  hgvsp: ENSP00000343339.4:p.Ala134del
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.400_402delGCC
  hgvsp: ENSP00000373762.3:p.Ala134del
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.357_359delGCC
  hgvsp: ENSP00000444853.1:p.Ala120del
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24482
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4814
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala134del
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: ACGC
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

12-133196447-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196447
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196447
    reference: chr 12
allele count: 1
allele frequency: 9.80622891660783e-6
allele num: 101976
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.399C>G
  hgvsp: ENSP00000373762.3:p.Asn133Lys
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.399C>G
  hgvsp: ENSP00000345095.5:p.Asn133Lys
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.327C>G
  hgvsp: ENSP00000405531.2:p.Asn109Lys
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.327C>G
  hgvsp: ENSP00000343904.5:p.Asn109Lys
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-139C>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.399C>G
  hgvsp: ENSP00000343339.4:p.Asn133Lys
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.266C>G
  hgvsp: ENSP00000437646.1:p.Asn89Lys
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.431C>G
  hgvsp: ENSP00000444477.1:p.Asn144Lys
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.356C>G
  hgvsp: ENSP00000444853.1:p.Asn119Lys
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.123C>G
  hgvsp: ENSP00000344502.4:p.Asn41Lys
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4644
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24602
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9231
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asn133Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

12-133196447-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196447
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196447
    reference: chr 12
allele count: 1
allele frequency: 9.80622891660783e-6
allele num: 101976
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.327C>T
  hgvsp: ENST00000449132.2:c.327C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.266C>T
  hgvsp: ENST00000535910.1:c.266C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.356C>T
  hgvsp: ENST00000536121.1:c.356C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-139C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.123C>T
  hgvsp: ENST00000351222.4:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.399C>T
  hgvsp: ENST00000343948.4:c.399C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.327C>T
  hgvsp: ENST00000350048.5:c.327C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.399C>T
  hgvsp: ENST00000348800.5:c.399C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.399C>T
  hgvsp: ENST00000389110.3:c.399C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.431C>T
  hgvsp: ENST00000542301.1:c.431C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11911
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4644
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7100
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asn133Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum

12-133196448-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196448
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196448
    reference: chr 12
allele count: 6
allele frequency: 5.907488726542347e-5
allele num: 101566
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.357G>C
  hgvsp: ENSP00000444853.1:p.Ala120Pro
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.328G>C
  hgvsp: ENSP00000343904.5:p.Ala110Pro
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.400G>C
  hgvsp: ENSP00000373762.3:p.Ala134Pro
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-138G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.267G>C
  hgvsp: ENSP00000437646.1:p.Ala90Pro
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.400G>C
  hgvsp: ENSP00000343339.4:p.Ala134Pro
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.400G>C
  hgvsp: ENSP00000345095.5:p.Ala134Pro
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.124G>C
  hgvsp: ENSP00000344502.4:p.Ala42Pro
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.328G>C
  hgvsp: ENSP00000405531.2:p.Ala110Pro
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.432G>C
  hgvsp: ENSP00000444477.1:p.Ala145Pro
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4649
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7035
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24585
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala134Pro
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

12-133196450-C-CAT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196450
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196452
    reference: chr 12
allele count: 1
allele frequency: 9.667440061871616e-6
allele num: 103440
alternate allele: CAT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.360_361insTA
  hgvsp: ENSP00000444853.1:p.Thr121IlefsTer21
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.331_332insTA
  hgvsp: ENSP00000405531.2:p.Thr111IlefsTer195
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.403_404insTA
  hgvsp: ENSP00000343339.4:p.Thr135IlefsTer21
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.331_332insTA
  hgvsp: ENSP00000343904.5:p.Thr111IlefsTer21
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.403_404insTA
  hgvsp: ENSP00000345095.5:p.Thr135IlefsTer21
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.127_128insTA
  hgvsp: ENSP00000344502.4:p.Thr43IlefsTer21
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.270_271insTA
  hgvsp: ENSP00000437646.1:p.Thr91IlefsTer21
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.435_436insTA
  hgvsp: ENSP00000444477.1:p.Thr146IlefsTer21
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-135_242-134insTA
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.403_404insTA
  hgvsp: ENSP00000373762.3:p.Thr135IlefsTer21
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2646
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6742
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3404
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12976
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6701
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 589
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr135IlefsTer21
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/12-133196451-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196451
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196451
    reference: chr 12
allele count: 254
allele frequency: 2.826241766067296e-3
allele num: 89872
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.270A>C
  hgvsp: ENSP00000437646.1:p.Thr91Pro
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-135A>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.435A>C
  hgvsp: ENSP00000444477.1:p.Thr146Pro
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.360A>C
  hgvsp: ENSP00000444853.1:p.Thr121Pro
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.403A>C
  hgvsp: ENSP00000343339.4:p.Thr135Pro
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.331A>C
  hgvsp: ENSP00000343904.5:p.Thr111Pro
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.127A>C
  hgvsp: ENSP00000344502.4:p.Thr43Pro
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.403A>C
  hgvsp: ENSP00000373762.3:p.Thr135Pro
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.403A>C
  hgvsp: ENSP00000345095.5:p.Thr135Pro
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.331A>C
  hgvsp: ENSP00000405531.2:p.Thr111Pro
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 22044
  bin: 2.25e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 3118
  bin: 3.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12688
  bin: 2.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6788
  bin: 1.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 6592
  bin: 1.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 3.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 4.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6332
  bin: 7.5e0
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1651
  bin: 1.75e1
  variant carriers: 12
hgvs: p.Thr135Pro
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum

12-133196463-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196463
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196463
    reference: chr 12
allele count: 1
allele frequency: 9.569377990430622e-6
allele num: 104500
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.415G>A
  hgvsp: ENSP00000373762.3:p.Asp139Asn
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.415G>A
  hgvsp: ENSP00000343339.4:p.Asp139Asn
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-123G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.372G>A
  hgvsp: ENSP00000444853.1:p.Asp125Asn
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.415G>A
  hgvsp: ENSP00000345095.5:p.Asp139Asn
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.447G>A
  hgvsp: ENSP00000444477.1:p.Asp150Asn
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.139G>A
  hgvsp: ENSP00000344502.4:p.Asp47Asn
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.282G>A
  hgvsp: ENSP00000437646.1:p.Asp95Asn
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.343G>A
  hgvsp: ENSP00000405531.2:p.Asp115Asn
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.343G>A
  hgvsp: ENSP00000343904.5:p.Asp115Asn
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17336
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6388
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4440
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asp139Asn
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

12-133196472-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196472
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196472
    reference: chr 12
allele count: 1
allele frequency: 9.667626984280438e-6
allele num: 103438
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.424T>G
  hgvsp: ENSP00000345095.5:p.Cys142Gly
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.352T>G
  hgvsp: ENSP00000405531.2:p.Cys118Gly
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.424T>G
  hgvsp: ENSP00000373762.3:p.Cys142Gly
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.424T>G
  hgvsp: ENSP00000343339.4:p.Cys142Gly
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-114T>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.381T>G
  hgvsp: ENSP00000444853.1:p.Cys128Gly
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.148T>G
  hgvsp: ENSP00000344502.4:p.Cys50Gly
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.352T>G
  hgvsp: ENSP00000343904.5:p.Cys118Gly
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.291T>G
  hgvsp: ENSP00000437646.1:p.Cys98Gly
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.456T>G
  hgvsp: ENSP00000444477.1:p.Cys153Gly
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24565
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6953
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3316
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1782
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Cys142Gly
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/12-133196474-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196474
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196474
    reference: chr 12
allele count: 75
allele frequency: 7.287354981635865e-4
allele num: 102918
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.354C>A
  hgvsp: ENSP00000343904.5:p.Cys118Ter
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.293C>A
  hgvsp: ENSP00000437646.1:p.Cys98Ter
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.426C>A
  hgvsp: ENSP00000373762.3:p.Cys142Ter
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.383C>A
  hgvsp: ENSP00000444853.1:p.Cys128Ter
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.458C>A
  hgvsp: ENSP00000444477.1:p.Cys153Ter
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.426C>A
  hgvsp: ENSP00000345095.5:p.Cys142Ter
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.354C>A
  hgvsp: ENSP00000405531.2:p.Cys118Ter
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.426C>A
  hgvsp: ENSP00000343339.4:p.Cys142Ter
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.150C>A
  hgvsp: ENSP00000344502.4:p.Cys50Ter
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-112C>A
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23943
  bin: 2.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 1.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3358
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 5570
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 17238
  bin: 2.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7100
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Cys142Ter
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

12-133196483-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196483
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196483
    reference: chr 12
allele count: 14
allele frequency: 1.388503193557345e-4
allele num: 100828
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.435G>A
  hgvsp: ENST00000348800.5:c.435G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.435G>A
  hgvsp: ENST00000389110.3:c.435G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.159G>A
  hgvsp: ENST00000351222.4:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.392G>A
  hgvsp: ENST00000536121.1:c.392G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.363G>A
  hgvsp: ENST00000350048.5:c.363G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.435G>A
  hgvsp: ENST00000343948.4:c.435G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.467G>A
  hgvsp: ENST00000542301.1:c.467G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.302G>A
  hgvsp: ENST00000535910.1:c.302G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-103G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.363G>A
  hgvsp: ENST00000449132.2:c.363G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16727
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3168
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8048
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7531
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21413
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1982
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly145Gly
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

12-133196492-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196492
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196492
    reference: chr 12
allele count: 2
allele frequency: 2.048424761358515e-5
allele num: 97636
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.311C>T
  hgvsp: ENST00000535910.1:c.311C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.444C>T
  hgvsp: ENST00000389110.3:c.444C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.401C>T
  hgvsp: ENST00000536121.1:c.401C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.444C>T
  hgvsp: ENST00000343948.4:c.444C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.372C>T
  hgvsp: ENST00000449132.2:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.372C>T
  hgvsp: ENST00000350048.5:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.476C>T
  hgvsp: ENST00000542301.1:c.476C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.444C>T
  hgvsp: ENST00000348800.5:c.444C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.168C>T
  hgvsp: ENST00000351222.4:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-94C>T
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18230
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9236
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15336
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10300
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1784
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1168
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asp148Asp
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ

12-133196494-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196494
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196494
    reference: chr 12
allele count: 14
allele frequency: 1.442555383822772e-4
allele num: 97050
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.313T>C
  hgvsp: ENSP00000437646.1:p.Met105Thr
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.446T>C
  hgvsp: ENSP00000345095.5:p.Met149Thr
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.446T>C
  hgvsp: ENSP00000373762.3:p.Met149Thr
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.374T>C
  hgvsp: ENSP00000405531.2:p.Met125Thr
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.478T>C
  hgvsp: ENSP00000444477.1:p.Met160Thr
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.403T>C
  hgvsp: ENSP00000444853.1:p.Met135Thr
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.446T>C
  hgvsp: ENSP00000343339.4:p.Met149Thr
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.170T>C
  hgvsp: ENSP00000344502.4:p.Met57Thr
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-92T>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.374T>C
  hgvsp: ENSP00000343904.5:p.Met125Thr
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11047
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2315
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1949
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 9502
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2896
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17503
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14838
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Met149Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP

12-133196495-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196495
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196494
    reference: chr 12
allele count: 1
allele frequency: 1.043340358491747e-5
allele num: 95846
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.405delC
  hgvsp: ENSP00000444853.1:p.Leu136TrpfsTer5
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.448delC
  hgvsp: ENSP00000345095.5:p.Leu150TrpfsTer5
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.480delC
  hgvsp: ENSP00000444477.1:p.Leu161TrpfsTer5
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.172delC
  hgvsp: ENSP00000344502.4:p.Leu58TrpfsTer5
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-90delC
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.448delC
  hgvsp: ENSP00000343339.4:p.Leu150TrpfsTer5
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.376delC
  hgvsp: ENSP00000405531.2:p.Leu126TrpfsTer179
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.448delC
  hgvsp: ENSP00000373762.3:p.Leu150TrpfsTer5
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.315delC
  hgvsp: ENSP00000437646.1:p.Leu106TrpfsTer5
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.376delC
  hgvsp: ENSP00000343904.5:p.Leu126TrpfsTer5
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 16399
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2880
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11977
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9828
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14215
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18900
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu150TrpfsTer5
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
reference allele: GC
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD

12-133196509-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196509
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196509
    reference: chr 12
allele count: 1
allele frequency: 1.152897230740852e-5
allele num: 86738
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.385+4G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.414+4G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.324+4G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.457+4G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.181+4G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.457+4G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-77G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.457+4G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.489+4G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.385+4G>C
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10718
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12663
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17032
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9613
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3790
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3887
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 550
  bin: 1.75e1
  variant carriers: 0
hgvs: c.457+4G>C
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

12-133196512-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196512
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196511
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 84224
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.457+8delT
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.181+8delT
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.324+8delT
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.457+8delT
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.385+8delT
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.489+8delT
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.385+8delT
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.457+8delT
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.414+8delT
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-73delT
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 8310
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18236
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4256
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9266
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13449
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 4.25e1
  variant carriers: 0
hgvs: c.457+8delT
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: GT
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

12-133196514-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196514
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196514
    reference: chr 12
allele count: 2
allele frequency: 2.460569375753549e-5
allele num: 81282
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.457+9G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.457+9G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.414+9G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.457+9G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.324+9G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.489+9G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.385+9G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.385+9G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-72G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.181+9G>C
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4784
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7874
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4839
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19236
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6994
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3844
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2952
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 865
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS

12-133196516-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196516
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196516
    reference: chr 12
allele count: 1
allele frequency: 1.291555808126469e-5
allele num: 77426
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.385+11G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.457+11G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.181+11G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.457+11G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.457+11G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.414+11G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.489+11G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.385+11G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-70G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.324+11G>A
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14895
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5926
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19940
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4928
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6785
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5467
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27729
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1025
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

12-133196520-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196520
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196520
    reference: chr 12
allele count: 3
allele frequency: 4.191817572099262e-5
allele num: 71568
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.181+15G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-66G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.457+15G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.385+15G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.385+15G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.324+15G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.414+15G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.457+15G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.457+15G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.489+15G>C
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5649
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6840
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5056
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20018
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4440
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1342
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7903
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

12-133196524-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196524
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196524
    reference: chr 12
allele count: 2
allele frequency: 3.074274471224791e-5
allele num: 65056
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.324+19G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.414+19G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.181+19G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.457+19G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.457+19G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.385+19G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.385+19G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.457+19G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.489+19G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-62G>C
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17497
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19401
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8049
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4745
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3479
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9106
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3981
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

12-133196525-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196525
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196525
    reference: chr 12
allele count: 1
allele frequency: 1.527230520174715e-5
allele num: 65478
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.457+20G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.324+20G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.414+20G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.385+20G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.489+20G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.457+20G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.385+20G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.181+20G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.457+20G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-61G>A
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19352
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17627
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4630
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 786
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1448
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

12-133196528-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196528
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196529
    reference: chr 12
allele count: 1
allele frequency: 1.688903901368012e-5
allele num: 59210
alternate allele: TG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.385+26dupG
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.457+26dupG
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.457+26dupG
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.489+26dupG
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.181+26dupG
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.457+26dupG
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.385+26dupG
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.414+26dupG
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-55dupG
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.324+26dupG
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9228
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4297
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19055
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4745
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23936
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5559
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1142
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum

12-133196534-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196534
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196534
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 51706
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.181+29G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.324+29G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.385+29G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.457+29G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-52G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.489+29G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.457+29G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.457+29G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.385+29G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.414+29G>A
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 16053
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10434
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4508
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21759
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3336
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 948
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 9.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

12-133196535-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196535
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196535
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 51894
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.385+30G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.489+30G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.457+30G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.385+30G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-51G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.181+30G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.457+30G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.457+30G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.414+30G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.324+30G>A
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22040
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4519
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15911
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10508
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3452
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5062
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1436
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

12-133196535-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196535
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196535
    reference: chr 12
allele count: 6
allele frequency: 1.156203029251937e-4
allele num: 51894
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.457+30G>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.324+30G>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-51G>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.385+30G>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.385+30G>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.181+30G>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.457+30G>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.414+30G>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.457+30G>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.489+30G>T
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15911
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10508
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4519
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22040
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1436
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11139
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

12-133196550-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196550
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196550
    reference: chr 12
allele count: 2
allele frequency: 4.398891479347205e-5
allele num: 45466
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.386-36G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-36G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.415-36G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.385+45G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.325-36G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.458-36G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.182-36G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.458-36G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.458-36G>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.490-36G>C
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24608
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13413
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11809
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4529
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3527
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD

12-133196550-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196550
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196550
    reference: chr 12
allele count: 1
allele frequency: 2.199445739673602e-5
allele num: 45466
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.458-36G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.385+45G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-36G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.415-36G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.490-36G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.182-36G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.325-36G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.458-36G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.458-36G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.386-36G>A
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11809
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13413
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24608
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4529
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12024
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3779
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3439
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4892
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

12-133196556-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196556
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196556
    reference: chr 12
allele count: 1
allele frequency: 2.253064167267484e-5
allele num: 44384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.458-30G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.458-30G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.325-30G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.415-30G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.385+51G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.386-30G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.182-30G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.458-30G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-30G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.490-30G>A
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12910
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2025
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11792
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3245
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5130
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1121
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

12-133196557-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196557
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196557
    reference: chr 12
allele count: 1
allele frequency: 2.239741981723705e-5
allele num: 44648
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.458-29C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.458-29C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.386-29C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.182-29C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.325-29C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.415-29C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.490-29C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.385+52C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.458-29C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-29C>T
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11805
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12793
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25314
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4796
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 831
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3414
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3260
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

12-133196558-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196558
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196558
    reference: chr 12
allele count: 1
allele frequency: 2.241348395194549e-5
allele num: 44616
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.458-28T>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.458-28T>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.415-28T>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-28T>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.458-28T>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.386-28T>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.385+53T>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.182-28T>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.490-28T>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.325-28T>C
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25424
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12700
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4838
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11770
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1017
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3246
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

12-133196564-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196564
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196564
    reference: chr 12
allele count: 1
allele frequency: 2.267985122017599e-5
allele num: 44092
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.458-22C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-22C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.386-57C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.415-22C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.458-22C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.458-22C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.182-22C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.386-22C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.325-22C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.490-22C>T
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4998
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25922
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11584
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12299
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3651
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3405
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1233
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3292
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

12-133196565-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196565
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196565
    reference: chr 12
allele count: 1
allele frequency: 2.268293789411605e-5
allele num: 44086
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242-21T>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.458-21T>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.458-21T>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.182-21T>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.386-56T>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.386-21T>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.415-21T>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.458-21T>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.325-21T>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.490-21T>C
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11539
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12291
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25967
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24679
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1051
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

12-133196586-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196586
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196586
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 44926
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.242G>T
  hgvsp: ENSP00000341419.4:p.Gly81Val
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.415G>T
  hgvsp: ENSP00000444853.1:p.Gly139Val
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.490G>T
  hgvsp: ENSP00000444477.1:p.Gly164Val
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.458G>T
  hgvsp: ENSP00000345095.5:p.Gly153Val
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.458G>T
  hgvsp: ENSP00000343339.4:p.Gly153Val
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.182G>T
  hgvsp: ENSP00000344502.4:p.Gly61Val
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.325G>T
  hgvsp: ENSP00000437646.1:p.Gly109Val
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.386G>T
  hgvsp: ENSP00000343904.5:p.Gly129Val
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.386-35G>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.458G>T
  hgvsp: ENSP00000373762.3:p.Gly153Val
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27513
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5787
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9675
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11710
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly153Val
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/12-133196588-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196588
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196588
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 45362
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.460C>A
  hgvsp: ENSP00000373762.3:p.Leu154Met
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.388C>A
  hgvsp: ENSP00000343904.5:p.Leu130Met
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.244C>A
  hgvsp: ENSP00000341419.4:p.Leu82Met
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.386-33C>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.460C>A
  hgvsp: ENSP00000343339.4:p.Leu154Met
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.460C>A
  hgvsp: ENSP00000345095.5:p.Leu154Met
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.327C>A
  hgvsp: ENSP00000437646.1:p.Leu110Met
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.417C>A
  hgvsp: ENSP00000444853.1:p.Leu140Met
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.492C>A
  hgvsp: ENSP00000444477.1:p.Leu165Met
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.184C>A
  hgvsp: ENSP00000344502.4:p.Leu62Met
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11710
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2227
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9419
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5912
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27620
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu154Met
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

12-133196593-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196593
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196593
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 46196
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.465G>A
  hgvsp: ENST00000389110.3:c.465G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.393G>A
  hgvsp: ENST00000350048.5:c.393G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.332G>A
  hgvsp: ENST00000535910.1:c.332G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.497G>A
  hgvsp: ENST00000542301.1:c.497G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.465G>A
  hgvsp: ENST00000343948.4:c.465G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.189G>A
  hgvsp: ENST00000351222.4:c.189G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.422G>A
  hgvsp: ENST00000536121.1:c.422G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.386-28G>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.465G>A
  hgvsp: ENST00000348800.5:c.465G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.249G>A
  hgvsp: ENST00000352418.4:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27736
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11837
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8765
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg155Arg
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

12-133196594-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196594
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196594
    reference: chr 12
allele count: 1
allele frequency: 2.155358220536253e-5
allele num: 46396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.498A>G
  hgvsp: ENSP00000444477.1:p.Thr167Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.466A>G
  hgvsp: ENSP00000345095.5:p.Thr156Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.466A>G
  hgvsp: ENSP00000343339.4:p.Thr156Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.423A>G
  hgvsp: ENSP00000444853.1:p.Thr142Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.466A>G
  hgvsp: ENSP00000373762.3:p.Thr156Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.333A>G
  hgvsp: ENSP00000437646.1:p.Thr112Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.190A>G
  hgvsp: ENSP00000344502.4:p.Thr64Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.386-27A>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.250A>G
  hgvsp: ENSP00000341419.4:p.Thr84Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.394A>G
  hgvsp: ENSP00000343904.5:p.Thr132Ala
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2194
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6237
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8648
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11892
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2243
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27745
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3406
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr156Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

12-133196596-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196596
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196596
    reference: chr 12
allele count: 1
allele frequency: 1.596525959512102e-5
allele num: 62636
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.396T>A
  hgvsp: ENST00000350048.5:c.396T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.500T>A
  hgvsp: ENST00000542301.1:c.500T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.468T>A
  hgvsp: ENST00000343948.4:c.468T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.335T>A
  hgvsp: ENST00000535910.1:c.335T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.425T>A
  hgvsp: ENST00000536121.1:c.425T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.468T>A
  hgvsp: ENST00000389110.3:c.468T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.252T>A
  hgvsp: ENST00000352418.4:c.252T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.468T>A
  hgvsp: ENST00000348800.5:c.468T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.386-25T>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.192T>A
  hgvsp: ENST00000351222.4:c.192T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6464
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16487
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4483
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2942
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21573
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8146
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr156Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum

12-133196596-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196596
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196596
    reference: chr 12
allele count: 41032
allele frequency: 6.550865317070056e-1
allele num: 62636
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.252T>C
  hgvsp: ENST00000352418.4:c.252T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.386-25T>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.425T>C
  hgvsp: ENST00000536121.1:c.425T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.335T>C
  hgvsp: ENST00000535910.1:c.335T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.396T>C
  hgvsp: ENST00000350048.5:c.396T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.468T>C
  hgvsp: ENST00000348800.5:c.468T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.468T>C
  hgvsp: ENST00000343948.4:c.468T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.500T>C
  hgvsp: ENST00000542301.1:c.500T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.468T>C
  hgvsp: ENST00000389110.3:c.468T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.192T>C
  hgvsp: ENST00000351222.4:c.192T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6464
  bin: 1.75e1
  variant carriers: 6067
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 351
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.25e1
  variant carriers: 420
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 3.25e1
  variant carriers: 408
genotype depth: GenotypeDepth
  all individuals: 4483
  bin: 2.5e0
  variant carriers: 2227
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 3.75e1
  variant carriers: 391
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 2.75e1
  variant carriers: 627
genotype depth: GenotypeDepth
  all individuals: 2942
  bin: 2.25e1
  variant carriers: 1779
genotype depth: GenotypeDepth
  all individuals: 21573
  bin: 7.5e0
  variant carriers: 14988
genotype depth: GenotypeDepth
  all individuals: 16487
  bin: 1.25e1
  variant carriers: 14435
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 5.75e1
  variant carriers: 508
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.25e1
  variant carriers: 460
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 4.75e1
  variant carriers: 503
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.75e1
  variant carriers: 292
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 6.75e1
  variant carriers: 472
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 9.75e1
  variant carriers: 514
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 408
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.25e1
  variant carriers: 215
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.25e1
  variant carriers: 475
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 514
genotype quality: GenotypeQuality
  all individuals: 3770
  bin: 3.25e1
  variant carriers: 3487
hgvs: p.Thr156Thr
num of homozygotes: 12819
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

12-133196597-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196597
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196597
    reference: chr 12
allele count: 3
allele frequency: 6.195019204559534e-5
allele num: 48426
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.193G>A
  hgvsp: ENSP00000344502.4:p.Gly65Arg
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.469G>A
  hgvsp: ENSP00000343339.4:p.Gly157Arg
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.253G>A
  hgvsp: ENSP00000341419.4:p.Gly85Arg
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.336G>A
  hgvsp: ENSP00000437646.1:p.Gly113Arg
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.469G>A
  hgvsp: ENSP00000373762.3:p.Gly157Arg
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.397G>A
  hgvsp: ENSP00000343904.5:p.Gly133Arg
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.469G>A
  hgvsp: ENSP00000345095.5:p.Gly157Arg
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.501G>A
  hgvsp: ENSP00000444477.1:p.Gly168Arg
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.426G>A
  hgvsp: ENSP00000444853.1:p.Gly143Arg
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.386-24G>A
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8025
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3233
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27304
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11826
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3415
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3720
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1191
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gly157Arg
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

12-133196607-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196607
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196607
    reference: chr 12
allele count: 1
allele frequency: 2.115238175818597e-5
allele num: 47276
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.479T>C
  hgvsp: ENSP00000373762.3:p.Val160Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.407T>C
  hgvsp: ENSP00000343904.5:p.Val136Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.386-14T>C
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.436T>C
  hgvsp: ENSP00000444853.1:p.Val146Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.511T>C
  hgvsp: ENSP00000444477.1:p.Val171Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.479T>C
  hgvsp: ENSP00000345095.5:p.Val160Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.479T>C
  hgvsp: ENSP00000343339.4:p.Val160Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.263T>C
  hgvsp: ENSP00000341419.4:p.Val88Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.346T>C
  hgvsp: ENSP00000437646.1:p.Val116Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.203T>C
  hgvsp: ENSP00000344502.4:p.Val68Ala
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3711
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11196
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27899
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8389
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7847
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val160Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

12-133196619-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196619
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196619
    reference: chr 12
allele count: 35
allele frequency: 7.564296520423601e-4
allele num: 46270
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.386-2A>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.491A>G
  hgvsp: ENSP00000373762.3:p.Gln164Arg
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.275A>G
  hgvsp: ENSP00000341419.4:p.Gln92Arg
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.358A>G
  hgvsp: ENSP00000437646.1:p.Gln120Arg
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.419A>G
  hgvsp: ENSP00000343904.5:p.Gln140Arg
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.491A>G
  hgvsp: ENSP00000345095.5:p.Gln164Arg
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.448A>G
  hgvsp: ENSP00000444853.1:p.Gln150Arg
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.491A>G
  hgvsp: ENSP00000343339.4:p.Gln164Arg
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.523A>G
  hgvsp: ENSP00000444477.1:p.Gln175Arg
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.215A>G
  hgvsp: ENSP00000344502.4:p.Gln72Arg
  variant of: http://identifiers.org/hgnc/15459
canonical: false
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28611
  bin: 7.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5151
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10682
  bin: 1.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3745
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8241
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 1.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 2186
  bin: 2.75e1
  variant carriers: 1
hgvs: c.386-2A>G
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

12-133196623-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196623
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196623
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 45852
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.423G>A
  hgvsp: ENST00000350048.5:c.423G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.495G>A
  hgvsp: ENST00000343948.4:c.495G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.527G>A
  hgvsp: ENST00000542301.1:c.527G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.495G>A
  hgvsp: ENST00000348800.5:c.495G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.279G>A
  hgvsp: ENST00000352418.4:c.279G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.219G>A
  hgvsp: ENST00000351222.4:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.452G>A
  hgvsp: ENST00000536121.1:c.452G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.495G>A
  hgvsp: ENST00000389110.3:c.495G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.388G>A
  hgvsp: ENSP00000405531.2:p.Ala130Thr
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.362G>A
  hgvsp: ENST00000535910.1:c.362G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28701
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8375
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10679
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala130Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

12-133196626-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196626
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196626
    reference: chr 12
allele count: 1
allele frequency: 2.208383021951327e-5
allele num: 45282
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.498C>T
  hgvsp: ENST00000348800.5:c.498C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.365C>T
  hgvsp: ENST00000535910.1:c.365C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.498C>T
  hgvsp: ENST00000389110.3:c.498C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.282C>T
  hgvsp: ENST00000352418.4:c.282C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.498C>T
  hgvsp: ENST00000343948.4:c.498C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.222C>T
  hgvsp: ENST00000351222.4:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.426C>T
  hgvsp: ENST00000350048.5:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.530C>T
  hgvsp: ENST00000542301.1:c.530C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.391C>T
  hgvsp: ENSP00000405531.2:p.Leu131Phe
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.455C>T
  hgvsp: ENST00000536121.1:c.455C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4917
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28722
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10668
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8542
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Leu131Phe
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

http://identifiers.org/exac.variant/12-133196629-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196629
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196629
    reference: chr 12
allele count: 1
allele frequency: 2.224100351407855e-5
allele num: 44962
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.501C>A
  hgvsp: ENST00000348800.5:c.501C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.429C>A
  hgvsp: ENST00000350048.5:c.429C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.394C>A
  hgvsp: ENSP00000405531.2:p.Gln132Lys
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.368C>A
  hgvsp: ENST00000535910.1:c.368C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.458C>A
  hgvsp: ENST00000536121.1:c.458C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.533C>A
  hgvsp: ENST00000542301.1:c.533C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.501C>A
  hgvsp: ENST00000389110.3:c.501C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.285C>A
  hgvsp: ENST00000352418.4:c.285C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.501C>A
  hgvsp: ENST00000343948.4:c.501C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.225C>A
  hgvsp: ENST00000351222.4:c.225C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8655
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10598
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28829
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4906
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3749
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gln132Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD

12-133196643-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196643
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196643
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 43346
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.239T>C
  hgvsp: ENSP00000344502.4:p.Val80Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.299T>C
  hgvsp: ENSP00000341419.4:p.Val100Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.515T>C
  hgvsp: ENSP00000345095.5:p.Val172Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.443T>C
  hgvsp: ENSP00000343904.5:p.Val148Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.408T>C
  hgvsp: ENST00000449132.2:c.408T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.547T>C
  hgvsp: ENSP00000444477.1:p.Val183Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.382T>C
  hgvsp: ENSP00000437646.1:p.Val128Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.515T>C
  hgvsp: ENSP00000343339.4:p.Val172Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.515T>C
  hgvsp: ENSP00000373762.3:p.Val172Ala
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.472T>C
  hgvsp: ENSP00000444853.1:p.Val158Ala
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28783
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4191
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9513
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10917
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val172Ala
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

12-133196647-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196647
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196647
    reference: chr 12
allele count: 2
allele frequency: 4.716313729189266e-5
allele num: 42406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.476C>T
  hgvsp: ENST00000536121.1:c.476C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.386C>T
  hgvsp: ENST00000535910.1:c.386C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.551C>T
  hgvsp: ENST00000542301.1:c.551C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.412C>T
  hgvsp: ENSP00000405531.2:p.Arg138Trp
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.303C>T
  hgvsp: ENST00000352418.4:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.519C>T
  hgvsp: ENST00000343948.4:c.519C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.519C>T
  hgvsp: ENST00000389110.3:c.519C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.519C>T
  hgvsp: ENST00000348800.5:c.519C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.243C>T
  hgvsp: ENST00000351222.4:c.243C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.447C>T
  hgvsp: ENST00000350048.5:c.447C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11029
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3812
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10048
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28524
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1627
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg138Trp
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

12-133196659-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196659
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196659
    reference: chr 12
allele count: 1
allele frequency: 2.536011361330899e-5
allele num: 39432
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.531G>A
  hgvsp: ENST00000343948.4:c.531G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.459G>A
  hgvsp: ENST00000350048.5:c.459G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.255G>A
  hgvsp: ENST00000351222.4:c.255G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.531G>A
  hgvsp: ENST00000389110.3:c.531G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.315G>A
  hgvsp: ENST00000352418.4:c.315G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.531G>A
  hgvsp: ENST00000348800.5:c.531G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.424G>A
  hgvsp: ENSP00000405531.2:p.Gly142Ser
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.563G>A
  hgvsp: ENST00000542301.1:c.563G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.398G>A
  hgvsp: ENST00000535910.1:c.398G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.488G>A
  hgvsp: ENST00000536121.1:c.488G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11805
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11110
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1917
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly142Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

12-133196671-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196671
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196671
    reference: chr 12
allele count: 1
allele frequency: 2.699492495410863e-5
allele num: 37044
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.543G>A
  hgvsp: ENST00000348800.5:c.543G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.267G>A
  hgvsp: ENST00000351222.4:c.267G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.471G>A
  hgvsp: ENST00000350048.5:c.471G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.327G>A
  hgvsp: ENST00000352418.4:c.327G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.543G>A
  hgvsp: ENST00000389110.3:c.543G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.500G>A
  hgvsp: ENST00000536121.1:c.500G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.575G>A
  hgvsp: ENST00000542301.1:c.575G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.410G>A
  hgvsp: ENST00000535910.1:c.410G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.436G>A
  hgvsp: ENSP00000405531.2:p.Gly146Ser
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.543G>A
  hgvsp: ENST00000343948.4:c.543G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15459
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14226
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26930
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly146Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

12-133196675-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196675
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196675
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 35750
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.547T>C
  hgvsp: ENSP00000345095.5:p.Ser183Pro
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.504T>C
  hgvsp: ENSP00000444853.1:p.Ser169Pro
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.475T>C
  hgvsp: ENSP00000343904.5:p.Ser159Pro
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.414T>C
  hgvsp: ENSP00000437646.1:p.Ser139Pro
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.547T>C
  hgvsp: ENSP00000343339.4:p.Ser183Pro
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.440T>C
  hgvsp: ENSP00000405531.2:p.Leu147Pro
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.547T>C
  hgvsp: ENSP00000373762.3:p.Ser183Pro
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.579T>C
  hgvsp: ENSP00000444477.1:p.Ser194Pro
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.271T>C
  hgvsp: ENSP00000344502.4:p.Ser91Pro
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.331T>C
  hgvsp: ENSP00000341419.4:p.Ser111Pro
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15213
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10931
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26503
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1957
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser183Pro
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

12-133196692-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196692
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196692
    reference: chr 12
allele count: 1
allele frequency: 3.738038277511962e-5
allele num: 26752
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.554+10C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.278+10C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.554+10C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.554+10C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.338+10C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.511+10C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.421+10C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.482+10C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.586+10C>T
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.447+10C>T
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19516
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25745
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19500
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

12-133196694-CCCCGGCCTGGGG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196694
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196682
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 26304
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19719
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7951
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25936
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19734
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: CCCCGGCCTGGGG
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum

12-133196695-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196695
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196695
    reference: chr 12
allele count: 1
allele frequency: 3.818251240931653e-5
allele num: 26190
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.338+13C>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.554+13C>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.421+13C>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.554+13C>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.482+13C>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.447+13C>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.278+13C>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.511+13C>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.554+13C>G
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.586+13C>G
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7868
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25995
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19765
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19841
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1925
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/12-133196696-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196696
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196696
    reference: chr 12
allele count: 757
allele frequency: 2.901050049819882e-2
allele num: 26094
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  hgvsc: ENST00000348800.5:c.554+14C>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  hgvsc: ENST00000542301.1:c.586+14C>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  hgvsc: ENST00000351222.4:c.278+14C>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  hgvsc: ENST00000352418.4:c.338+14C>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  hgvsc: ENST00000389110.3:c.554+14C>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  hgvsc: ENST00000350048.5:c.482+14C>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  hgvsc: ENST00000449132.2:c.447+14C>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  hgvsc: ENST00000343948.4:c.554+14C>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  hgvsc: ENST00000536121.1:c.511+14C>A
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  hgvsc: ENST00000535910.1:c.421+14C>A
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 3.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 1.75e1
  variant carriers: 152
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 2.25e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25954
  bin: 7.5e0
  variant carriers: 645
genotype depth: GenotypeDepth
  all individuals: 19664
  bin: 2.5e0
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 7883
  bin: 1.25e1
  variant carriers: 382
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 2.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1366
  bin: 9.75e1
  variant carriers: 792
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 4.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 5.75e1
  variant carriers: 54
genotype quality: GenotypeQuality
  all individuals: 1900
  bin: 2.5e0
  variant carriers: 1
num of homozygotes: 16
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

12-133196700-CCTGGGGCCCAGCCTCCCCT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133196700
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 133196681
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 25352
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000405531
  ensembl transcript: ENST00000449132
  gene symbol: P2RX2
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444477
  ensembl transcript: ENST00000542301
  gene symbol: P2RX2
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000341419
  ensembl transcript: ENST00000352418
  gene symbol: P2RX2
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000444853
  ensembl transcript: ENST00000536121
  gene symbol: P2RX2
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343339
  ensembl transcript: ENST00000343948
  gene symbol: P2RX2
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000343904
  ensembl transcript: ENST00000350048
  gene symbol: P2RX2
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000345095
  ensembl transcript: ENST00000348800
  gene symbol: P2RX2
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000373762
  ensembl transcript: ENST00000389110
  gene symbol: P2RX2
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000344502
  ensembl transcript: ENST00000351222
  gene symbol: P2RX2
  variant of: http://identifiers.org/hgnc/15459
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187848
  ensembl protein: ENSP00000437646
  ensembl transcript: ENST00000535910
  gene symbol: P2RX2
  variant of: http://identifiers.org/hgnc/15459
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7588
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26145
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: CCTGGGGCCCAGCCTCCCCT

GenotypeQuality
all individuals: 96
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 730
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2501
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11170
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 906
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1417
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1870
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4423
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1433
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 749
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3696
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22540
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7684
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7104
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10424
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 712
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4958
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.30941469163284e-4
allele num: 15274
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55284
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.131e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.04e-1

QD
type: SiteQuality
SIO_000300: 1.044e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -5.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.31e-1

DP
type: SiteQuality
SIO_000300: 1.12617e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.6e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1671
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 589
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3933
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2508
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20709
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11537
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3163
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 826
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 811
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 679
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4744
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3671
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4756
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6954
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15136
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 714
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.314060446780552e-4
allele num: 7610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54732
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.098453e6

VQSLOD
type: SiteQuality
SIO_000300: 4.63e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.96e0

MQRankSum
type: SiteQuality
SIO_000300: 4.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.12e-1

FS
type: SiteQuality
SIO_000300: 2.098e0

QD
type: SiteQuality
SIO_000300: 1.624e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.6e-2

GenotypeQuality
all individuals: 4691
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1267
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11760
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 541
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 819
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21872
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2489
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3574
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54826
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.691800736576855e-5
allele num: 10318
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15150
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4814
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7004
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 714
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.355e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

DP
type: SiteQuality
SIO_000300: 1.099971e6

VQSLOD
type: SiteQuality
SIO_000300: 3.63e-1

QD
type: SiteQuality
SIO_000300: 8.970000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: -3.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.39e-1

GenotypeQuality
all individuals: 683
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 829
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3561
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1987
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1309
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4700
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3905
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1566
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 514
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3254
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 712
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7010
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7620
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.819174094960888e-5
allele num: 54970
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4830
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15172
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.812e0

DP
type: SiteQuality
SIO_000300: 1.098691e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.9e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.64e-1

QD
type: SiteQuality
SIO_000300: 1.257e1

VQSLOD
type: SiteQuality
SIO_000300: 1.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.519e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.74e-1

MQ
type: SiteQuality
SIO_000300: 5.943e1

GenotypeQuality
all individuals: 3629
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 918
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 564
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1999
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2471
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1639
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20505
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 806
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 679
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4726
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3141
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.321877065432915e-4
allele num: 15130
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54844
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4738
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6960
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-3

DP
type: SiteQuality
SIO_000300: 1.096699e6

VQSLOD
type: SiteQuality
SIO_000300: 6.860000000000001e-1

FS
type: SiteQuality
SIO_000300: 1.483e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.68e0

QD
type: SiteQuality
SIO_000300: 1.159e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.659999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 116
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 813
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1471
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4722
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7666
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.818843215714806e-5
allele num: 54980
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7002
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15124
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.97e-1

DP
type: SiteQuality
SIO_000300: 1.099974e6

MQRankSum
type: SiteQuality
SIO_000300: -2.584e0

MQ
type: SiteQuality
SIO_000300: 5.907e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.86e0

QD
type: SiteQuality
SIO_000300: 1.367e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.54e-1

FS
type: SiteQuality
SIO_000300: 3.682e0

VQSLOD
type: SiteQuality
SIO_000300: -2.604e0

GenotypeQuality
all individuals: 1360
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1904
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4690
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7006
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7638
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.819703752229137e-5
allele num: 54954
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15082
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.53e-1

QD
type: SiteQuality
SIO_000300: 1.178e1

FS
type: SiteQuality
SIO_000300: 1.871e0

MQRankSum
type: SiteQuality
SIO_000300: -5.669999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.94e-1

DP
type: SiteQuality
SIO_000300: 1.10555e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.43e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 782
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11221
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 54

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1629
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15106
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7672
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4702
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.426126640045636e-4
allele num: 7012
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 53
allele frequency: 9.620271545777971e-4
allele num: 55092
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.931620629708325e-4
allele num: 10354
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.82e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.229e1

MQRankSum
type: SiteQuality
SIO_000300: 3.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.108157e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-2

GenotypeQuality
all individuals: 11238
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3338
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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: 2

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: 86
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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: 4146
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 716
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.621220351258374e-5
allele num: 55230
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7686
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 710
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7022
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4690
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15114
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.81e-1

DP
type: SiteQuality
SIO_000300: 1.11485e6

VQSLOD
type: SiteQuality
SIO_000300: -1.715e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-3

FS
type: SiteQuality
SIO_000300: 1.1992e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.064e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.42e-1

QD
type: SiteQuality
SIO_000300: 7.59e0

GenotypeQuality
all individuals: 118
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 91
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GenotypeQuality
all individuals: 492
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GenotypeQuality
all individuals: 3627
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variant carriers: 0

GenotypeQuality
all individuals: 1065
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 27415
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 369
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variant carriers: 0

GenotypeQuality
all individuals: 2500
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.398013531020584e-5
allele num: 55576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15104
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4682
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7744
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7068
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 710
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.55e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.26e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.329e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 9.31e-1

DP
type: SiteQuality
SIO_000300: 1.138872e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 9.7e-2

QD
type: SiteQuality
SIO_000300: 1.177e1

GenotypeQuality
all individuals: 840
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2729
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variant carriers: 0

GenotypeQuality
all individuals: 158
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2259
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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: 407
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 921
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variant carriers: 0

GenotypeQuality
all individuals: 92
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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
all individuals: 3885
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variant carriers: 0

GenotypeQuality
all individuals: 812
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4694
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10454
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 722
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7118
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.790895089365665e-5
allele num: 55838
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7810
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15110
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.65e-1

QD
type: SiteQuality
SIO_000300: 1.707e1

MQ
type: SiteQuality
SIO_000300: 5.922e1

FS
type: SiteQuality
SIO_000300: 1.685e0

MQRankSum
type: SiteQuality
SIO_000300: -4.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.27e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.17e-1

DP
type: SiteQuality
SIO_000300: 1.157924e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

GenotypeQuality
all individuals: 423
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 746
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GenotypeQuality
all individuals: 128
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 718
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.78782136088962e-5
allele num: 55934
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15110
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4666
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7808
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10456
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7148
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.766e0

DP
type: SiteQuality
SIO_000300: 1.165064e6

MQ
type: SiteQuality
SIO_000300: 5.878e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.46e-1

QD
type: SiteQuality
SIO_000300: 3.35e0

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
all individuals: 946
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GenotypeQuality
all individuals: 639
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 718
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7134
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.788652786721042e-5
allele num: 55908
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4580
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15100
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7822
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10450
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.069e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.734e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.333e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.1e-2

QD
type: SiteQuality
SIO_000300: 3.54e0

MQ
type: SiteQuality
SIO_000300: 5.82e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.0e-1

DP
type: SiteQuality
SIO_000300: 1.166822e6

GenotypeQuality
all individuals: 30259
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1069
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
all individuals: 465
bin: 1.25e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 95
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1682
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10460
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7150
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.785459220111413e-5
allele num: 56008
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15096
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4658
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7824
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

MQ
type: SiteQuality
SIO_000300: 5.89e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.386e0

MQRankSum
type: SiteQuality
SIO_000300: -5.56e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.723e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.1714e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.83e-1

QD
type: SiteQuality
SIO_000300: 1.04e0

GenotypeQuality
all individuals: 1281
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 733
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 2659
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variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7154
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4692
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56064
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10484
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15090
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 718
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7836
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

QD
type: SiteQuality
SIO_000300: 1.287e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

DP
type: SiteQuality
SIO_000300: 1.171862e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.96e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.736e0

VQSLOD
type: SiteQuality
SIO_000300: 2.62e-1

GenotypeQuality
all individuals: 119
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2628
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variant carriers: 0

GenotypeQuality
all individuals: 2136
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variant carriers: 0

GenotypeQuality
all individuals: 885
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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
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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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variant carriers: 0

GenotypeQuality
all individuals: 773
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 764
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4588
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 718
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7144
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.786288449858883e-5
allele num: 55982
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15086
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7834
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10472
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

MQRankSum
type: SiteQuality
SIO_000300: -5.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.62e-1

DP
type: SiteQuality
SIO_000300: 1.17168e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e0

QD
type: SiteQuality
SIO_000300: 1.306e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.95e0

MQ
type: SiteQuality
SIO_000300: 5.863e1

GenotypeQuality
all individuals: 9213
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2487
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29825
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2136
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1099
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 138
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1672
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 773
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1499
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variant carriers: 0

GenotypeQuality
all individuals: 764
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 753
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
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variant carriers: 0

GenotypeQuality
all individuals: 4087
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 718
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4588
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7144
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.628662335940607e-5
allele num: 15086
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7834
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55982
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10472
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.17168e6

MQ
type: SiteQuality
SIO_000300: 5.863e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.95e0

QD
type: SiteQuality
SIO_000300: 1.306e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.62e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.22e-1

GenotypeQuality
all individuals: 29569
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
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variant carriers: 0

GenotypeQuality
all individuals: 2626
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variant carriers: 0

GenotypeQuality
all individuals: 794
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 980
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1667
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 895
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variant carriers: 0

GenotypeQuality
all individuals: 1108
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1513
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.784758165268606e-5
allele num: 56030
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7156
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7832
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10464
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15080
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4698
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.659000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.42e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.174951e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.500000000000001e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.78e-1

QD
type: SiteQuality
SIO_000300: 9.26e0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56030
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4698
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.276813074565884e-4
allele num: 7832
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7156
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15080
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10464
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.500000000000001e-3

QD
type: SiteQuality
SIO_000300: 9.26e0

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

DP
type: SiteQuality
SIO_000300: 1.174951e6

VQSLOD
type: SiteQuality
SIO_000300: 3.78e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e-1

FS
type: SiteQuality
SIO_000300: 8.659000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.42e-1

GenotypeQuality
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bin: 3.25e1
variant carriers: 1

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 978
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GenotypeQuality
all individuals: 141
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15076
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10468
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 712
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.376729514660549e-5
allele num: 55796
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7110
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.276161306789178e-4
allele num: 7836
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 4.378283712784588e-4
allele num: 4568
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.736e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.286e0

VQSLOD
type: SiteQuality
SIO_000300: -1.599e1

DP
type: SiteQuality
SIO_000300: 1.178026e6

QD
type: SiteQuality
SIO_000300: 3.9e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

MQ
type: SiteQuality
SIO_000300: 5.899e1

MQRankSum
type: SiteQuality
SIO_000300: -9.1e-2

FS
type: SiteQuality
SIO_000300: 5.4086e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e0

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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variant carriers: 0

GenotypeQuality
all individuals: 9124
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GenotypeQuality
all individuals: 212
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GenotypeQuality
all individuals: 189
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 559
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56918
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4858
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7412
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10538
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7884
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.622516556291391e-5
allele num: 15100
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.733e0

QD
type: SiteQuality
SIO_000300: 1.51e1

MQ
type: SiteQuality
SIO_000300: 5.859e1

MQRankSum
type: SiteQuality
SIO_000300: -9.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.83e0

DP
type: SiteQuality
SIO_000300: 1.207944e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.35e-1

GenotypeQuality
all individuals: 6576
bin: 2.5e0
variant carriers: 8

GenotypeQuality
all individuals: 1235
bin: 1.25e1
variant carriers: 15

GenotypeQuality
all individuals: 2810
bin: 6.75e1
variant carriers: 14

GenotypeQuality
all individuals: 93
bin: 8.75e1
variant carriers: 8

GenotypeQuality
all individuals: 23478
bin: 6.25e1
variant carriers: 11

GenotypeQuality
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bin: 5.75e1
variant carriers: 17

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.25e1
variant carriers: 27

GenotypeQuality
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bin: 4.75e1
variant carriers: 22

GenotypeQuality
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bin: 9.75e1
variant carriers: 39

GenotypeQuality
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variant carriers: 19

GenotypeQuality
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variant carriers: 5

GenotypeQuality
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variant carriers: 15

GenotypeQuality
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bin: 2.75e1
variant carriers: 16

GenotypeQuality
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bin: 3.25e1
variant carriers: 30

GenotypeQuality
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bin: 3.75e1
variant carriers: 24

GenotypeQuality
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variant carriers: 11

GenotypeQuality
all individuals: 265
bin: 8.25e1
variant carriers: 5

GenotypeQuality
all individuals: 528
bin: 7.75e1
variant carriers: 9

Latino
type: Population
allele count: 25
allele frequency: 2.703871944624703e-3
allele num: 9246
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 144
allele frequency: 2.89890083343399e-3
allele num: 49674
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 5.534034311012728e-4
allele num: 14456
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 25
allele frequency: 8.514986376021799e-3
allele num: 2936
num of homozygotes: 0

African
type: Population
allele count: 24
allele frequency: 4.028197381671702e-3
allele num: 5958
num of homozygotes: 0

East Asian
type: Population
allele count: 26
allele frequency: 3.717472118959108e-3
allele num: 6994
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 3.289473684210526e-3
allele num: 608
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.210389e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.36e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.38e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.672e2

MQRankSum
type: SiteQuality
SIO_000300: 1.81e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.747e0

FS
type: SiteQuality
SIO_000300: 2.83097e2

MQ
type: SiteQuality
SIO_000300: 5.94e1

QD
type: SiteQuality
SIO_000300: 1.45e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.45e0

GenotypeQuality
all individuals: 4951
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 924
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 468
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GenotypeQuality
all individuals: 428
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 728
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7614
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.256597134958532e-4
allele num: 7958
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15036
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10576
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4788
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57800
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.043e0

QD
type: SiteQuality
SIO_000300: 1.236e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.46e-1

FS
type: SiteQuality
SIO_000300: 1.0241e1

MQ
type: SiteQuality
SIO_000300: 5.948e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.276e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.41e0

MQRankSum
type: SiteQuality
SIO_000300: -4.47e-1

DP
type: SiteQuality
SIO_000300: 1.280646e6

GenotypeQuality
all individuals: 419
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variant carriers: 0

GenotypeQuality
all individuals: 680
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variant carriers: 0

GenotypeQuality
all individuals: 94
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variant carriers: 0

GenotypeQuality
all individuals: 240
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variant carriers: 0

GenotypeQuality
all individuals: 1009
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 167
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variant carriers: 0

GenotypeQuality
all individuals: 82
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GenotypeQuality
all individuals: 214
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 425
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variant carriers: 0

GenotypeQuality
all individuals: 119
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variant carriers: 0

GenotypeQuality
all individuals: 37446
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10442
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4696
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7886
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.746358841814816e-5
allele num: 57262
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 728
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.263967e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e-1

FS
type: SiteQuality
SIO_000300: 1.237e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.85e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.3e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.81e0

QD
type: SiteQuality
SIO_000300: 1.512e1

GenotypeQuality
all individuals: 182
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1817
bin: 7.5e0
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GenotypeQuality
all individuals: 189
bin: 9.75e1
variant carriers: 77

GenotypeQuality
all individuals: 4717
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
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variant carriers: 0

GenotypeQuality
all individuals: 10829
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variant carriers: 0

GenotypeQuality
all individuals: 433
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variant carriers: 1

GenotypeQuality
all individuals: 941
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variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 133
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variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 4.25e1
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GenotypeQuality
all individuals: 279
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 964
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variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 9.25e1
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GenotypeQuality
all individuals: 349
bin: 5.75e1
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GenotypeQuality
all individuals: 821
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GenotypeQuality
all individuals: 36671
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variant carriers: 0

GenotypeQuality
all individuals: 400
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variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 3.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 34
allele frequency: 5.962820063135742e-4
allele num: 57020
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7850
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7474
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 41
allele frequency: 8.828596037898364e-3
allele num: 4644
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14836
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 718
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.15e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.57e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.67e-1

QD
type: SiteQuality
SIO_000300: 1.058e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.75e-1

DP
type: SiteQuality
SIO_000300: 1.257725e6

GenotypeQuality
all individuals: 4470
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 321
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GenotypeQuality
all individuals: 163
bin: 1.25e1
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GenotypeQuality
all individuals: 863
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GenotypeQuality
all individuals: 289
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GenotypeQuality
all individuals: 34224
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GenotypeQuality
all individuals: 121
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 79
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GenotypeQuality
all individuals: 99
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7290
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.252146536920435e-4
allele num: 55904
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 7
allele frequency: 1.58156348847718e-3
allele num: 4426
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7726
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 696
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.215212e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.699999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.81e-1

FS
type: SiteQuality
SIO_000300: 1.155e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-3

MQ
type: SiteQuality
SIO_000300: 5.907e1

QD
type: SiteQuality
SIO_000300: 1.991e1

GenotypeQuality
all individuals: 2312
bin: 7.5e0
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 90
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GenotypeQuality
all individuals: 320
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GenotypeQuality
all individuals: 105
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GenotypeQuality
all individuals: 596
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GenotypeQuality
all individuals: 286
bin: 4.75e1
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GenotypeQuality
all individuals: 200
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variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4184
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7022
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7488
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 682
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14290
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.692080487354624e-5
allele num: 54170
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.5e-2

DP
type: SiteQuality
SIO_000300: 1.151788e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.575e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

QD
type: SiteQuality
SIO_000300: 1.187e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.84e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.11e0

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

GenotypeQuality
all individuals: 29280
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 235
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GenotypeQuality
all individuals: 592
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GenotypeQuality
all individuals: 320
bin: 8.25e1
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GenotypeQuality
all individuals: 117
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 1277
bin: 3.25e1
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GenotypeQuality
all individuals: 302
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GenotypeQuality
all individuals: 198
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7448
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9728
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6988
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 7.235890014471779e-4
allele num: 4146
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 2.043849869936826e-4
allele num: 53820
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14248
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.08e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.7e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.81e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

QD
type: SiteQuality
SIO_000300: 9.15e0

DP
type: SiteQuality
SIO_000300: 1.134455e6

GenotypeQuality
all individuals: 712
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1903
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27289
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1432
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2581
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 567
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 658
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53116
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6918
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14130
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4084
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.045150501672241e-4
allele num: 9568
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.961e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.047e0

DP
type: SiteQuality
SIO_000300: 1.111912e6

MQRankSum
type: SiteQuality
SIO_000300: 1.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.36e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.908e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.72e-1

FS
type: SiteQuality
SIO_000300: 2.128e0

QD
type: SiteQuality
SIO_000300: 2.93e0

GenotypeQuality
all individuals: 234
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 2484
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 69
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 590
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6154
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47968
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.504127269998499e-5
allele num: 13326
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6660
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.53e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.15e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

DP
type: SiteQuality
SIO_000300: 9.50797e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.900000000000001e-3

FS
type: SiteQuality
SIO_000300: 3.403e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.953e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.55e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 284
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 434
bin: 7.75e1
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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
all individuals: 2287
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variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 5.75e1
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GenotypeQuality
all individuals: 265
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 216
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variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 4.75e1
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GenotypeQuality
all individuals: 100
bin: 9.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13124
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5976
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8142
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46552
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 572
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.46e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 9.05813e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.05e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

QD
type: SiteQuality
SIO_000300: 1.576e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

GenotypeQuality
all individuals: 262
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1083
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 102
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variant carriers: 2

GenotypeQuality
all individuals: 69
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 480
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variant carriers: 0

GenotypeQuality
all individuals: 264
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variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2088
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5762
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6260
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3232
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 564
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7776
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.230649118893598e-5
allele num: 44830
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.777259293824856e-5
allele num: 12858
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.31e0

MQ
type: SiteQuality
SIO_000300: 5.916e1

QD
type: SiteQuality
SIO_000300: 1.204e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

DP
type: SiteQuality
SIO_000300: 8.61636e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.44e-2

FS
type: SiteQuality
SIO_000300: 9.74e-1

GenotypeQuality
all individuals: 6423
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 3164
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1272
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 256
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GenotypeQuality
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GenotypeQuality
all individuals: 408
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GenotypeQuality
all individuals: 263
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1700
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GenotypeQuality
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GenotypeQuality
all individuals: 440
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 67
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 1
allele frequency: 8.00640512409928e-5
allele num: 12490
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2974
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7318
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5472
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42656
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5966
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

FS
type: SiteQuality
SIO_000300: 8.616e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.568e0

VQSLOD
type: SiteQuality
SIO_000300: -7.861e-1

DP
type: SiteQuality
SIO_000300: 8.21142e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.54e-2

QD
type: SiteQuality
SIO_000300: 9.32e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.96e-1

GenotypeQuality
all individuals: 227
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 2.5e0
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GenotypeQuality
all individuals: 67
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variant carriers: 1

GenotypeQuality
all individuals: 1532
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variant carriers: 0

GenotypeQuality
all individuals: 3521
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GenotypeQuality
all individuals: 105
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variant carriers: 2

GenotypeQuality
all individuals: 413
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GenotypeQuality
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GenotypeQuality
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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: 257
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 7.621176709683975e-5
allele num: 39364
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2560
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 488
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5570
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6682
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4954
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11950
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.089e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.77e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.58927e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

VQSLOD
type: SiteQuality
SIO_000300: 4.9e-1

GenotypeQuality
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bin: 5.75e1
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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GenotypeQuality
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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: 362
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6030
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5110
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 9.624639076034649e-4
allele num: 2078
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11312
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35600
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4488
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 438
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.12e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.11e-1

FS
type: SiteQuality
SIO_000300: 5.423e0

VQSLOD
type: SiteQuality
SIO_000300: -1.012e0

MQ
type: SiteQuality
SIO_000300: 5.378e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.9e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.606e0

DP
type: SiteQuality
SIO_000300: 7.08418e5

QD
type: SiteQuality
SIO_000300: 1.552e1

GenotypeQuality
all individuals: 9211
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2141
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 104
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 262
bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 125
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GenotypeQuality
all individuals: 26334
bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2104
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.794076557697681e-5
allele num: 35790
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6064
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5154
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11372
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.254e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.1335e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

DP
type: SiteQuality
SIO_000300: 7.06336e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.11e-2

QD
type: SiteQuality
SIO_000300: 1.982e1

GenotypeQuality
all individuals: 248
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3496
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.104625892579944e-5
allele num: 32210
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4156
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5324
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1662
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4744
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10720
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 5.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.38e-2

QD
type: SiteQuality
SIO_000300: 1.28e1

MQRankSum
type: SiteQuality
SIO_000300: 7.84e-1

DP
type: SiteQuality
SIO_000300: 6.68081e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.2e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.808e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.1e-2

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 344
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1226
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10088
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3788
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27856
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4366
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4038
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.53e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.48e0

VQSLOD
type: SiteQuality
SIO_000300: -2.522e0

FS
type: SiteQuality
SIO_000300: 4.039e0

MQRankSum
type: SiteQuality
SIO_000300: -9.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.59e-2

DP
type: SiteQuality
SIO_000300: 6.28268e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4382
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4090
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3802
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 342
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27960
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1214
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.26e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.47e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.26e-1

QD
type: SiteQuality
SIO_000300: 1.357e1

FS
type: SiteQuality
SIO_000300: 3.024e0

MQRankSum
type: SiteQuality
SIO_000300: 7.83e-1

DP
type: SiteQuality
SIO_000300: 6.25789e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.84e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5062
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1214
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4090
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 5.938242280285036e-4
allele num: 10104
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27960
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3802
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4382
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 342
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.16e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.47e-2

DP
type: SiteQuality
SIO_000300: 6.25789e5

VQSLOD
type: SiteQuality
SIO_000300: 5.26e-1

FS
type: SiteQuality
SIO_000300: 3.024e0

MQRankSum
type: SiteQuality
SIO_000300: 7.83e-1

QD
type: SiteQuality
SIO_000300: 1.357e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.84e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 260
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.135991397137894e-5
allele num: 24178
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3412
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3606
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9570
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.870264064293915e-4
allele num: 3484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 920
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 296
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.1765e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 8.100000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.47e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 5.94847e5

MQRankSum
type: SiteQuality
SIO_000300: 5.29e-1

QD
type: SiteQuality
SIO_000300: 1.009e1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9570
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.773155851358847e-4
allele num: 3606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24178
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 920
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3484
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 296
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3412
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.1765e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.100000000000001e-1

VQSLOD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3630
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 3.010234798314269e-4
allele num: 3322
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 23472
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
num of homozygotes: 0

South Asian
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allele count: 0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.264e0

DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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GenotypeQuality
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bin: 7.5e0
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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bin: 7.25e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
type: Population
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allele frequency: 0.0e0
allele num: 9498
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 3298
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: 308
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.230476351637195e-5
allele num: 23638
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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FS
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
all individuals: 364
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GenotypeQuality
all individuals: 90
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3684
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3296
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23606
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.052631578947368e-4
allele num: 9500
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 308
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 912
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.948e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.41e-1

DP
type: SiteQuality
SIO_000300: 5.96257e5

VQSLOD
type: SiteQuality
SIO_000300: 1.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

FS
type: SiteQuality
SIO_000300: 4.203e0

QD
type: SiteQuality
SIO_000300: 1.353e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-1

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11641
bin: 7.5e0
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23256
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3228
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3194
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.645502645502646e-4
allele num: 3780
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 302
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9446
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 3.471e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.699e0

MQ
type: SiteQuality
SIO_000300: 5.866e1

DP
type: SiteQuality
SIO_000300: 5.97304e5

VQSLOD
type: SiteQuality
SIO_000300: -1.676e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.55e-2

QD
type: SiteQuality
SIO_000300: 7.1e0

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
all individuals: 5378
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3788
num of homozygotes: 0

European (Finnish)
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: 9444
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3186
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3222
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.301815366084488e-5
allele num: 23246
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 302
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.563e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.24e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.94e-1

FS
type: SiteQuality
SIO_000300: 4.117e0

DP
type: SiteQuality
SIO_000300: 5.98182e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.55e-2

QD
type: SiteQuality
SIO_000300: 5.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 117
bin: 9.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4032
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9472
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3132
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3302
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 310
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23718
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 960
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -6.899e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.04e-1

QD
type: SiteQuality
SIO_000300: 1.826e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.15e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.18787e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.04e-1

GenotypeDepth
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 5986
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
all individuals: 25489
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 304
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3346
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3142
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23962
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 986
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4118
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9504
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-2

DP
type: SiteQuality
SIO_000300: 6.22315e5

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

MQ
type: SiteQuality
SIO_000300: 5.682e1

QD
type: SiteQuality
SIO_000300: 6.01e0

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.195e0

GenotypeQuality
all individuals: 1140
bin: 6.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24464
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1018
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 310
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4180
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3450
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3202
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.26e0

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.81e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.03e-1

DP
type: SiteQuality
SIO_000300: 6.32037e5

VQSLOD
type: SiteQuality
SIO_000300: -1.782e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

QD
type: SiteQuality
SIO_000300: 2.098e1

GenotypeQuality
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bin: 7.5e0
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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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 313
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3218
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9584
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: 316
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.070335395636601e-5
allele num: 24568
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.141e0

VQSLOD
type: SiteQuality
SIO_000300: -9.14e-2

MQRankSum
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DP
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BaseQRankSum
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.81e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-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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bin: 4.25e1
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GenotypeQuality
all individuals: 632
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1786
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5514
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4862
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5180
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 446
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10750
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.932723326881342e-5
allele num: 34098
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.79e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e-1

DP
type: SiteQuality
SIO_000300: 9.49134e5

FS
type: SiteQuality
SIO_000300: 1.104e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.558e-1

QD
type: SiteQuality
SIO_000300: 2.189e1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

GenotypeQuality
all individuals: 821
bin: 8.25e1
variant carriers: 811

GenotypeQuality
all individuals: 802
bin: 5.75e1
variant carriers: 772

GenotypeQuality
all individuals: 4546
bin: 2.5e0
variant carriers: 208

GenotypeQuality
all individuals: 2640
bin: 3.75e1
variant carriers: 2519

GenotypeQuality
all individuals: 1699
bin: 1.25e1
variant carriers: 1424

GenotypeQuality
all individuals: 4073
bin: 1.75e1
variant carriers: 3647

GenotypeQuality
all individuals: 2602
bin: 2.75e1
variant carriers: 2275

GenotypeQuality
all individuals: 1637
bin: 4.75e1
variant carriers: 1591

GenotypeQuality
all individuals: 8146
bin: 2.25e1
variant carriers: 4169

GenotypeQuality
all individuals: 632
bin: 7.75e1
variant carriers: 607

GenotypeQuality
all individuals: 928
bin: 8.75e1
variant carriers: 924

GenotypeQuality
all individuals: 1036
bin: 4.25e1
variant carriers: 998

GenotypeQuality
all individuals: 2224
bin: 6.25e1
variant carriers: 875

GenotypeQuality
all individuals: 472
bin: 7.25e1
variant carriers: 443

GenotypeQuality
all individuals: 1211
bin: 5.25e1
variant carriers: 1171

GenotypeQuality
all individuals: 2596
bin: 7.5e0
variant carriers: 1099

GenotypeQuality
all individuals: 943
bin: 9.25e1
variant carriers: 942

GenotypeQuality
all individuals: 17476
bin: 9.75e1
variant carriers: 17461

GenotypeQuality
all individuals: 734
bin: 6.75e1
variant carriers: 631

European (Finnish)
type: Population
allele count: 1080
allele frequency: 6.047032474804032e-1
allele num: 1786
num of homozygotes: 266

Latino
type: Population
allele count: 4173
allele frequency: 8.055984555984556e-1
allele num: 5180
num of homozygotes: 1639

European (Non-Finnish)
type: Population
allele count: 20688
allele frequency: 6.067218018652121e-1
allele num: 34098
num of homozygotes: 5616

African
type: Population
allele count: 4419
allele frequency: 8.014145810663765e-1
allele num: 5514
num of homozygotes: 1744

Other
type: Population
allele count: 287
allele frequency: 6.434977578475336e-1
allele num: 446
num of homozygotes: 86

South Asian
type: Population
allele count: 6477
allele frequency: 6.025116279069768e-1
allele num: 10750
num of homozygotes: 1930

East Asian
type: Population
allele count: 3908
allele frequency: 8.037844508432743e-1
allele num: 4862
num of homozygotes: 1538

BaseQRankSum
type: SiteQuality
SIO_000300: -5.36e-1

FS
type: SiteQuality
SIO_000300: 1.104e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.558e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.189e1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

DP
type: SiteQuality
SIO_000300: 9.49134e5

VQSLOD
type: SiteQuality
SIO_000300: 6.79e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.1e-2

GenotypeQuality
all individuals: 506
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25691
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5132
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 707
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 343
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GenotypeQuality
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GenotypeQuality
all individuals: 642
bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7490
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variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2560
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 664
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variant carriers: 0

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

GenotypeQuality
all individuals: 1646
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variant carriers: 0

GenotypeQuality
all individuals: 1039
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variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 9.25e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9840
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4500
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3684
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1222
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 9.541984732824427e-4
allele num: 3144
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25696
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.5e-2

FS
type: SiteQuality
SIO_000300: 8.159000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

QD
type: SiteQuality
SIO_000300: 3.095e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.47e-2

DP
type: SiteQuality
SIO_000300: 6.85499e5

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.517e0

GenotypeQuality
all individuals: 6914
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1184
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variant carriers: 0

GenotypeQuality
all individuals: 2419
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variant carriers: 0

GenotypeQuality
all individuals: 2361
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variant carriers: 0

GenotypeQuality
all individuals: 28389
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variant carriers: 0

GenotypeQuality
all individuals: 112
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variant carriers: 0

GenotypeQuality
all individuals: 808
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variant carriers: 0

GenotypeQuality
all individuals: 2482
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variant carriers: 0

GenotypeQuality
all individuals: 118
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variant carriers: 0

GenotypeQuality
all individuals: 110
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GenotypeQuality
all individuals: 3137
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variant carriers: 0

GenotypeQuality
all individuals: 189
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variant carriers: 0

GenotypeQuality
all individuals: 1456
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variant carriers: 1

GenotypeQuality
all individuals: 554
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GenotypeQuality
all individuals: 638
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variant carriers: 1

GenotypeQuality
all individuals: 337
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variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24960
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1174
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4402
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9754
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.306878306878307e-4
allele num: 3024
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 336
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.57e0

DP
type: SiteQuality
SIO_000300: 6.84894e5

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.227e0

FS
type: SiteQuality
SIO_000300: 3.646e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.68e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.322e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.12e-1

GenotypeQuality
all individuals: 1018
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1638
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1173
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 181
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 662
bin: 9.75e1
variant carriers: 31

GenotypeQuality
all individuals: 312
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2108
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31135
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variant carriers: 1

GenotypeQuality
all individuals: 7934
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variant carriers: 0

GenotypeQuality
all individuals: 296
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variant carriers: 1

GenotypeQuality
all individuals: 8060
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variant carriers: 0

GenotypeQuality
all individuals: 440
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GenotypeQuality
all individuals: 115
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variant carriers: 1

GenotypeQuality
all individuals: 1891
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variant carriers: 0

GenotypeQuality
all individuals: 331
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variant carriers: 2

GenotypeQuality
all individuals: 207
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 125
bin: 5.75e1
variant carriers: 1

Latino
type: Population
allele count: 4
allele frequency: 1.380262249827467e-3
allele num: 2898
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9680
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3546
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1126
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4326
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 320
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 31
allele frequency: 1.27184705013539e-3
allele num: 24374
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.96e-1

QD
type: SiteQuality
SIO_000300: 1.033e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.76e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.01e0

DP
type: SiteQuality
SIO_000300: 6.91646e5

GenotypeQuality
all individuals: 247
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
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variant carriers: 0

GenotypeQuality
all individuals: 8125
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GenotypeQuality
all individuals: 455
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GenotypeQuality
all individuals: 31376
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variant carriers: 0

GenotypeQuality
all individuals: 2161
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variant carriers: 0

GenotypeQuality
all individuals: 110
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GenotypeQuality
all individuals: 113
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GenotypeQuality
all individuals: 255
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GenotypeQuality
all individuals: 320
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GenotypeQuality
all individuals: 1548
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variant carriers: 0

GenotypeQuality
all individuals: 911
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GenotypeQuality
all individuals: 1955
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GenotypeQuality
all individuals: 2027
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variant carriers: 0

GenotypeQuality
all individuals: 262
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GenotypeQuality
all individuals: 328
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GenotypeQuality
all individuals: 1164
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8003
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GenotypeQuality
all individuals: 631
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 320
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1120
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4294
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2848
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24114
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9626
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.88e0

MQRankSum
type: SiteQuality
SIO_000300: -8.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.75e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.61e-1

MQ
type: SiteQuality
SIO_000300: 5.569e1

VQSLOD
type: SiteQuality
SIO_000300: -1.353e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.219e0

DP
type: SiteQuality
SIO_000300: 6.88645e5

GenotypeQuality
all individuals: 317
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8304
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 521
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1938
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 112
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GenotypeQuality
all individuals: 215
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GenotypeQuality
all individuals: 624
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GenotypeQuality
all individuals: 110
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GenotypeQuality
all individuals: 2139
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GenotypeQuality
all individuals: 257
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GenotypeQuality
all individuals: 1142
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
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variant carriers: 0

GenotypeQuality
all individuals: 7666
bin: 6.25e1
variant carriers: 0

Other
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: 4.210526315789474e-5
allele num: 23750
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9602
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4252
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3470
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1100
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2794
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.91e-1

DP
type: SiteQuality
SIO_000300: 6.84656e5

VQSLOD
type: SiteQuality
SIO_000300: -7.57e-1

FS
type: SiteQuality
SIO_000300: 2.172e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.96e-1

QD
type: SiteQuality
SIO_000300: 3.13e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.83e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.149e0

GenotypeQuality
all individuals: 31671
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variant carriers: 0

GenotypeQuality
all individuals: 8474
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GenotypeQuality
all individuals: 229
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GenotypeQuality
all individuals: 171
bin: 8.25e1
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GenotypeQuality
all individuals: 318
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GenotypeQuality
all individuals: 316
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GenotypeQuality
all individuals: 271
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 109
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GenotypeQuality
all individuals: 1834
bin: 3.25e1
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GenotypeQuality
all individuals: 1123
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 620
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GenotypeQuality
all individuals: 111
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GenotypeQuality
all individuals: 218
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GenotypeQuality
all individuals: 770
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GenotypeQuality
all individuals: 1497
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variant carriers: 0

GenotypeQuality
all individuals: 2040
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 5.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23580
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2760
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1094
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4216
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.923976608187135e-4
allele num: 3420
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9576
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.517e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.85e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.43e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.5e-2

DP
type: SiteQuality
SIO_000300: 6.8246e5

QD
type: SiteQuality
SIO_000300: 5.77e0

GenotypeQuality
all individuals: 169
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 614
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GenotypeQuality
all individuals: 9401
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GenotypeQuality
all individuals: 158
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GenotypeQuality
all individuals: 2001
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GenotypeQuality
all individuals: 304
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GenotypeQuality
all individuals: 589
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GenotypeQuality
all individuals: 104
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GenotypeQuality
all individuals: 459
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GenotypeQuality
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GenotypeQuality
all individuals: 7010
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GenotypeQuality
all individuals: 1665
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GenotypeQuality
all individuals: 2166
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1456
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
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GenotypeQuality
all individuals: 32167
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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Other
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num of homozygotes: 0

South Asian
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DP
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VQSLOD
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FS
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MQ
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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QD
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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South Asian
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allele frequency: 1.114330287497214e-4
allele num: 8974
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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ReadPosRankSum
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SIO_000300: 2.96e-1

DP
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QD
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VQSLOD
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MQRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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MQ
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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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: 266
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 5.295488244016098e-5
allele num: 18884
num of homozygotes: 0

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

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

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

MQRankSum
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SIO_000300: -1.48e0

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

ClippingRankSum
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DP
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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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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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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VQSLOD
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SIO_000300: 2.03e-1

ClippingRankSum
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FS
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BaseQRankSum
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QD
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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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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Other
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East Asian
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African
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European (Finnish)
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South Asian
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European (Non-Finnish)
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allele num: 12856
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Latino
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InbreedingCoeff
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QD
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DP
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FS
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BaseQRankSum
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MQRankSum
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MQ
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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East Asian
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South Asian
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European (Non-Finnish)
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European (Finnish)
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BaseQRankSum
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ClippingRankSum
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FS
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QD
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ReadPosRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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DP
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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European (Finnish)
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East Asian
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Latino
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African
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South Asian
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ReadPosRankSum
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MQ
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VQSLOD
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FS
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DP
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MQRankSum
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BaseQRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 381
bin: 6.75e1
variant carriers: 37

GenotypeQuality
all individuals: 171
bin: 8.25e1
variant carriers: 52

GenotypeQuality
all individuals: 171
bin: 8.75e1
variant carriers: 84

GenotypeQuality
all individuals: 4226
bin: 1.75e1
variant carriers: 35

GenotypeQuality
all individuals: 187
bin: 7.25e1
variant carriers: 34

Latino
type: Population
allele count: 23
allele frequency: 2.228682170542636e-2
allele num: 1032
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 576
allele frequency: 4.575059571088165e-2
allele num: 12590
num of homozygotes: 12

Other
type: Population
allele count: 11
allele frequency: 4.782608695652174e-2
allele num: 230
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1634
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 11
allele frequency: 2.422907488986784e-2
allele num: 454
num of homozygotes: 0

African
type: Population
allele count: 21
allele frequency: 8.152173913043478e-3
allele num: 2576
num of homozygotes: 0

South Asian
type: Population
allele count: 115
allele frequency: 1.517550804961731e-2
allele num: 7578
num of homozygotes: 3

QD
type: SiteQuality
SIO_000300: 1.445e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.87e0

FS
type: SiteQuality
SIO_000300: 1.757e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.31e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 4.79961e5