22-36124985-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36124985
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36124985
    reference: chr 22
allele count: 1
allele frequency: 9.005925899241701e-6
allele num: 111038
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128313
  ensembl protein: ENSP00000249044
  ensembl transcript: ENST00000249044
  gene symbol: APOL5
  hgvsc: ENST00000249044.2:c.*6+34G>A
  variant of: http://identifiers.org/hgnc/14869
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2318
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 650
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.75e1
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genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 8.25e1
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genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2097
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 62642
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6108
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 1
  allele frequency: 9.010632546404758e-5
  allele num: 11098
  num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/22-36124988-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36124988
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36124988
    reference: chr 22
allele count: 8
allele frequency: 7.257815760346924e-5
allele num: 110226
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128313
  ensembl protein: ENSP00000249044
  ensembl transcript: ENST00000249044
  gene symbol: APOL5
  hgvsc: ENST00000249044.2:c.*6+37C>A
  variant of: http://identifiers.org/hgnc/14869
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11585
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
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genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 1382
  bin: 5.25e1
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genotype quality: GenotypeQuality
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  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 437
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genotype quality: GenotypeQuality
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  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 6037
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2066
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 784
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6060
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8084
  num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

22-36124991-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36124991
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36124991
    reference: chr 22
allele count: 1
allele frequency: 9.13575735428467e-6
allele num: 109460
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128313
  ensembl protein: ENSP00000249044
  ensembl transcript: ENST00000249044
  gene symbol: APOL5
  hgvsc: ENST00000249044.2:c.*6+40C>G
  variant of: http://identifiers.org/hgnc/14869
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10839
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13914
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.75e1
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genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 195
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 44
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 508
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num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 1.61363196282192e-5
  allele num: 61972
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8008
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 12076
  num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

22-36124996-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36124996
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36124996
    reference: chr 22
allele count: 2
allele frequency: 1.851166234727879e-5
allele num: 108040
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128313
  ensembl protein: ENSP00000249044
  ensembl transcript: ENST00000249044
  gene symbol: APOL5
  hgvsc: ENST00000249044.2:c.*6+45A>G
  variant of: http://identifiers.org/hgnc/14869
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12825
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 3241
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num of homozygotes: 0
population: Latino
  type: Population
  allele count: 2
  allele frequency: 1.840264998159735e-4
  allele num: 10868
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 5996
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9550
  num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

22-36140194-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140194
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140194
    reference: chr 22
allele count: 1
allele frequency: 8.66265874322147e-6
allele num: 115438
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.*48G>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2336G>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.*48G>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.*58G>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.*48G>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.*58G>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.*58G>C
  variant of: http://identifiers.org/hgnc/9906
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8764
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13173
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18203
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2972
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3630
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3243
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25012
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4328
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5301
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2827
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4102
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/22-36140198-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140198
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140198
    reference: chr 22
allele count: 4
allele frequency: 3.448454230391227e-5
allele num: 115994
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.*44T>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.*54T>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.*44T>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.*44T>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.*54T>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.*54T>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.*54T>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2332T>G
  variant of: http://identifiers.org/hgnc/9906
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21770
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8545
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9459
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2997
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3547
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3373
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/22-36140205-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140205
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140205
    reference: chr 22
allele count: 1
allele frequency: 8.603334652511313e-6
allele num: 116234
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.*37G>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.*37G>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.*47G>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.*47G>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.*47G>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2325G>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.*47G>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.*37G>T
  variant of: http://identifiers.org/hgnc/9906
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25948
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5088
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7094
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3285
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14805
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2314
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1380
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1860
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3071
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3235
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3275
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35826
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

22-36140208-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140208
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140208
    reference: chr 22
allele count: 3
allele frequency: 2.574930476877124e-5
allele num: 116508
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.*34G>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2322G>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.*34G>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.*44G>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.*44G>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.*44G>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.*34G>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.*44G>A
  variant of: http://identifiers.org/hgnc/9906
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3884
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27441
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38214
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 860
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD

22-36140210-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140210
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140210
    reference: chr 22
allele count: 1
allele frequency: 8.56956775100264e-6
allele num: 116692
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.*32A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.*42A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.*32A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.*42A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.*42A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.*42A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.*32A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2320A>G
  variant of: http://identifiers.org/hgnc/9906
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5656
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15639
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3359
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39568
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 771
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2453
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1075
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1381
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3019
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD

22-36140215-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140215
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140216
    reference: chr 22
allele count: 1
allele frequency: 8.559005785887911e-6
allele num: 116836
alternate allele: TG
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.*26dupC
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.*36dupC
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.*36dupC
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.*36dupC
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.*36dupC
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.*26dupC
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.*36dupC
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.*26dupC
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2314dupC
  variant of: http://identifiers.org/hgnc/9906
canonical: false
consequence: 3' UTR
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29435
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4721
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3526
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41072
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2836
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 866
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 752
  bin: 7.75e1
  variant carriers: 0
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: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

22-36140215-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140215
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140214
    reference: chr 22
allele count: 1
allele frequency: 8.559005785887911e-6
allele num: 116836
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.*36delC
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.*26delC
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.*26delC
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.*26delC
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2314delC
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.*36delC
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.*36delC
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.*36delC
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.*36delC
  variant of: http://identifiers.org/hgnc/9906
canonical: false
consequence: 3' UTR
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4721
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3526
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29435
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2085
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 867
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2836
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: TG
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS

22-36140216-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140216
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140216
    reference: chr 22
allele count: 2
allele frequency: 1.712270127735352e-5
allele num: 116804
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.*36C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.*36C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.*36C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2314C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.*36C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.*26C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.*26C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.*26C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.*36C>T
  variant of: http://identifiers.org/hgnc/9906
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16364
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4513
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29602
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1287
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41624
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 746
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

22-36140220-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140220
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140220
    reference: chr 22
allele count: 8
allele frequency: 6.822096771442703e-5
allele num: 117266
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.*32C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.*22C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.*32C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2310C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.*32C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.*22C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.*32C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.*22C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.*32C>T
  variant of: http://identifiers.org/hgnc/9906
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1965
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3826
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16939
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3534
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30408
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2627
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4754
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum

22-36140222-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140222
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140222
    reference: chr 22
allele count: 1
allele frequency: 8.521516829995738e-6
allele num: 117350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.*20G>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2308G>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.*20G>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.*30G>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.*30G>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.*20G>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.*30G>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.*30G>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.*30G>C
  variant of: http://identifiers.org/hgnc/9906
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17180
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3592
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3573
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30516
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4741
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1373
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1045
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum

22-36140225-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140225
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140225
    reference: chr 22
allele count: 1
allele frequency: 8.504413790757403e-6
allele num: 117586
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.*17A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.*27A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.*17A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2305A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.*27A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.*27A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.*27A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.*17A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.*27A>G
  variant of: http://identifiers.org/hgnc/9906
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3070
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31036
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3636
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 774
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2434
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum

22-36140228-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140228
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140228
    reference: chr 22
allele count: 1
allele frequency: 8.490117503226245e-6
allele num: 117784
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.*24G>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.*24G>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.*14G>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.*24G>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.*24G>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2302G>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.*14G>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.*14G>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.*24G>C
  variant of: http://identifiers.org/hgnc/9906
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1716
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31484
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 793
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4794
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 757
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

22-36140235-A-AG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140235
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140236
    reference: chr 22
allele count: 1
allele frequency: 8.4530853761623e-6
allele num: 118300
alternate allele: AG
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.*16dupC
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.*6dupC
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2294dupC
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.*6dupC
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.*16dupC
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.*16dupC
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.*16dupC
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.*16dupC
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.*6dupC
  variant of: http://identifiers.org/hgnc/9906
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3756
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18405
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1375
  bin: 9.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

22-36140243-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140243
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140243
    reference: chr 22
allele count: 1
allele frequency: 8.42971305256769e-6
allele num: 118628
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1103G>A
  hgvsp: ENST00000405409.2:c.1103G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2287G>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1112G>A
  hgvsp: ENST00000414461.2:c.1112G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.*9G>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.*9G>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1112G>A
  hgvsp: ENST00000359369.4:c.1112G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.*9G>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.*9G>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.*9G>A
  variant of: http://identifiers.org/hgnc/9906
canonical: false
consequence: stop retained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32822
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18783
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 785
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ter368Ter
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/22-36140245-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140245
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140245
    reference: chr 22
allele count: 3
allele frequency: 2.527678074920378e-5
allele num: 118686
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.*7G>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.*7G>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1110G>T
  hgvsp: ENST00000414461.2:c.1110G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.*7G>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.*7G>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.*7G>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1110G>T
  hgvsp: ENST00000359369.4:c.1110G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1101G>T
  hgvsp: ENST00000405409.2:c.1101G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2285G>T
  variant of: http://identifiers.org/hgnc/9906
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3838
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18928
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32806
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4964
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 919
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48262
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr367Thr
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

22-36140245-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140245
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140245
    reference: chr 22
allele count: 6
allele frequency: 5.055356149840757e-5
allele num: 118686
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1110G>A
  hgvsp: ENST00000359369.4:c.1110G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.*7G>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.*7G>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.*7G>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1110G>A
  hgvsp: ENST00000414461.2:c.1110G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1101G>A
  hgvsp: ENST00000405409.2:c.1101G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.*7G>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.*7G>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2285G>A
  variant of: http://identifiers.org/hgnc/9906
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3838
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32806
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18928
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 919
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48262
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr367Thr
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

22-36140246-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140246
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140246
    reference: chr 22
allele count: 7
allele frequency: 5.898511889714681e-5
allele num: 118674
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.*6C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2284C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1109C>T
  hgvsp: ENSP00000407855.2:p.Thr370Met
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.*6C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1109C>T
  hgvsp: ENSP00000352328.4:p.Thr370Met
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.*6C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.*6C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1100C>T
  hgvsp: ENSP00000384944.2:p.Thr367Met
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.*6C>T
  variant of: http://identifiers.org/hgnc/9906
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18984
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32778
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1380
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr367Met
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

22-36140258-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140258
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140258
    reference: chr 22
allele count: 11
allele frequency: 9.263157894736843e-5
allele num: 118750
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1097C>T
  hgvsp: ENSP00000352328.4:p.Pro366Leu
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1125C>T
  hgvsp: ENST00000416721.2:c.1125C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.1071C>T
  hgvsp: ENST00000262829.7:c.1071C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.686C>T
  hgvsp: ENST00000495377.2:c.686C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1137C>T
  hgvsp: ENST00000449924.2:c.1137C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1088C>T
  hgvsp: ENSP00000384944.2:p.Pro363Leu
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.1068C>T
  hgvsp: ENST00000397303.2:c.1068C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1097C>T
  hgvsp: ENSP00000407855.2:p.Pro366Leu
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2272C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1350C>T
  hgvsp: ENST00000438146.2:c.1350C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3867
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32681
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19377
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro366Leu
num of homozygotes: 1
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum

22-36140282-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140282
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140282
    reference: chr 22
allele count: 1
allele frequency: 8.59963537546008e-6
allele num: 116284
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1326A>G
  hgvsp: ENST00000438146.2:c.1326A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1101A>G
  hgvsp: ENST00000416721.2:c.1101A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2248A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.1044A>G
  hgvsp: ENST00000397303.2:c.1044A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.662A>G
  hgvsp: ENST00000495377.2:c.662A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1113A>G
  hgvsp: ENST00000449924.2:c.1113A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1064A>G
  hgvsp: ENSP00000384944.2:p.Glu355Gly
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1073A>G
  hgvsp: ENSP00000352328.4:p.Glu358Gly
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.1047A>G
  hgvsp: ENST00000262829.7:c.1047A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1073A>G
  hgvsp: ENSP00000407855.2:p.Glu358Gly
  variant of: http://identifiers.org/hgnc/9906
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2513
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2744
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29294
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 511
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu358Gly
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/22-36140296-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140296
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140296
    reference: chr 22
allele count: 1
allele frequency: 9.01079493232893e-6
allele num: 110978
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.1030G>T
  hgvsp: ENSP00000380470.2:p.Ala344Ser
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1050G>T
  hgvsp: ENSP00000384944.2:p.Trp350Cys
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2234G>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.1033G>T
  hgvsp: ENSP00000262829.7:p.Ala345Ser
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1059G>T
  hgvsp: ENSP00000407855.2:p.Trp353Cys
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1312G>T
  hgvsp: ENSP00000413035.2:p.Ala438Ser
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.648G>T
  hgvsp: ENSP00000474464.1:p.Ala217Ser
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1099G>T
  hgvsp: ENSP00000391670.2:p.Ala367Ser
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1087G>T
  hgvsp: ENSP00000405651.2:p.Ala363Ser
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1059G>T
  hgvsp: ENSP00000352328.4:p.Trp353Cys
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7161
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5061
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23065
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3676
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala438Ser
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP

22-36140313-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140313
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140313
    reference: chr 22
allele count: 1
allele frequency: 1.006583053167717e-5
allele num: 99346
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1050-17C>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1099-17C>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1087-17C>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1059-17C>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.1030-17C>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1312-17C>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.1033-17C>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.648-17C>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1059-17C>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2234-17C>G
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3335
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10165
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2354
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20700
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11074
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10503
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2530
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

22-36140313-GAT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140313
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140311
    reference: chr 22
allele count: 1
allele frequency: 1.006583053167717e-5
allele num: 99346
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.1030-19_1030-18delAT
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1087-19_1087-18delAT
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1050-19_1050-18delAT
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2234-19_2234-18delAT
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.1033-19_1033-18delAT
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1059-19_1059-18delAT
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1099-19_1099-18delAT
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1312-19_1312-18delAT
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.648-19_648-18delAT
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1059-19_1059-18delAT
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3335
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10165
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2354
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20700
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11074
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10503
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4031
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4057
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: GAT
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

22-36140324-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140324
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140324
    reference: chr 22
allele count: 1
allele frequency: 1.068581564830843e-5
allele num: 93582
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1312-28A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1099-28A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.1033-28A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1059-28A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1087-28A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.1030-28A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1059-28A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1050-28A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.648-28A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2234-28A>G
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6154
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26349
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11885
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5856
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5644
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 631
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/22-36140326-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140326
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140326
    reference: chr 22
allele count: 1
allele frequency: 1.082110548413626e-5
allele num: 92412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.1030-30T>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.648-30T>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1087-30T>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1050-30T>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2234-30T>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1059-30T>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1059-30T>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1099-30T>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1312-30T>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.1033-30T>G
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26578
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6466
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12252
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5007
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1067
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3161
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 781
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum

22-36140331-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140331
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140331
    reference: chr 22
allele count: 1
allele frequency: 1.137915339098771e-5
allele num: 87880
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1059-35C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1087-35C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.1033-35C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1059-35C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.648-35C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2234-35C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1312-35C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1099-35C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1050-35C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.1030-35C>T
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3620
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2433
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13671
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8518
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25852
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3786
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1613
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24609
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7676
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

22-36140333-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140333
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140333
    reference: chr 22
allele count: 2
allele frequency: 2.289272469209285e-5
allele num: 87364
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1050-37A>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1312-37A>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1099-37A>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2234-37A>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1059-37A>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.648-37A>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1059-37A>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.1030-37A>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1087-37A>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.1033-37A>C
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25609
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14022
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3444
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8747
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2520
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1537
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7734
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 832
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

22-36140334-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140334
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140334
    reference: chr 22
allele count: 1
allele frequency: 1.174674027957242e-5
allele num: 85130
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2234-38C>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1099-38C>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1059-38C>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1050-38C>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.648-38C>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1059-38C>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.1030-38C>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.1033-38C>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1312-38C>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1087-38C>A
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24838
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14786
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9546
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4841
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1357
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7793
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

22-36140336-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140336
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140336
    reference: chr 22
allele count: 2
allele frequency: 2.370005214011471e-5
allele num: 84388
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1312-40A>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1059-40A>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1050-40A>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1059-40A>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.1030-40A>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1087-40A>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1099-40A>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.1033-40A>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.648-40A>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2234-40A>T
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2677
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24524
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9731
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2997
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 732
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1358
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum

22-36140336-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140336
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140336
    reference: chr 22
allele count: 1
allele frequency: 1.185002607005735e-5
allele num: 84388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1059-40A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.1030-40A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1050-40A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1087-40A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1099-40A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2234-40A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.648-40A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1312-40A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1059-40A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.1033-40A>G
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2677
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2997
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24524
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9731
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 732
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3838
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2326
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

22-36140344-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36140344
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36140344
    reference: chr 22
allele count: 6
allele frequency: 7.872982548222017e-5
allele num: 76210
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1099-48C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1312-48C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1050-48C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.1033-48C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1059-48C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2234-48C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1087-48C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1059-48C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.1030-48C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.648-48C>T
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18577
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2787
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21596
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9624
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3849
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1613
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3786
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1359
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 576
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

22-36141926-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36141926
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36141926
    reference: chr 22
allele count: 344
allele frequency: 2.840815247910679e-3
allele num: 121092
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1311+44C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.647+44C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2233+44C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1098+44C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.1029+44C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.1032+44C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1086+44C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1058+44C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1049+44C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1058+44C>T
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 2.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 32006
  bin: 9.75e1
  variant carriers: 261
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2766
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 3430
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2690
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 705
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 4
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

22-36141935-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36141935
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36141935
    reference: chr 22
allele count: 1
allele frequency: 8.255729476256522e-6
allele num: 121128
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.1029+35A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1086+35A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1098+35A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1311+35A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1058+35A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.1032+35A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1058+35A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.647+35A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1049+35A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2233+35A>G
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3207
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3053
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31929
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3446
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD

22-36141938-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36141938
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36141938
    reference: chr 22
allele count: 1
allele frequency: 8.255729476256522e-6
allele num: 121128
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1311+32A>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1058+32A>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1086+32A>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.1029+32A>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1098+32A>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.1032+32A>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1058+32A>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2233+32A>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1049+32A>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.647+32A>T
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3445
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3291
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31929
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

22-36141941-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36141941
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36141941
    reference: chr 22
allele count: 8
allele frequency: 6.603929337956083e-5
allele num: 121140
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1058+29A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.647+29A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1086+29A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1058+29A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1098+29A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.1032+29A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1311+29A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2233+29A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1049+29A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.1029+29A>G
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3373
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3445
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31928
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5530
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

22-36141943-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36141943
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36141943
    reference: chr 22
allele count: 1
allele frequency: 8.254639107178234e-6
allele num: 121144
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.1032+27A>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1311+27A>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.1029+27A>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.647+27A>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1058+27A>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1098+27A>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2233+27A>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1058+27A>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1049+27A>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1086+27A>C
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31926
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3404
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3156
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3445
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50472
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum

22-36141946-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36141946
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36141946
    reference: chr 22
allele count: 1
allele frequency: 8.253276550790664e-6
allele num: 121164
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1058+24T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.1029+24T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.647+24T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2233+24T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1058+24T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1311+24T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.1032+24T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1049+24T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1098+24T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1086+24T>C
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3464
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3183
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3445
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31925
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5727
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum

22-36141962-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36141962
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36141962
    reference: chr 22
allele count: 1
allele frequency: 8.247422680412371e-6
allele num: 121250
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1049+8T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.647+8T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.1032+8T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1098+8T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1086+8T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1058+8T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.1029+8T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1058+8T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1311+8T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2233+8T>C
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3531
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3445
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31925
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
hgvs: c.1311+8T>C
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: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/22-36141975-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36141975
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36141975
    reference: chr 22
allele count: 1
allele frequency: 8.245246615326264e-6
allele num: 121282
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1053G>T
  hgvsp: ENST00000359369.4:c.1053G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1081G>T
  hgvsp: ENSP00000405651.2:p.Ala361Ser
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2228G>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1053G>T
  hgvsp: ENST00000414461.2:c.1053G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1306G>T
  hgvsp: ENSP00000413035.2:p.Ala436Ser
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1044G>T
  hgvsp: ENST00000405409.2:c.1044G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.642G>T
  hgvsp: ENSP00000474464.1:p.Ala215Ser
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.1027G>T
  hgvsp: ENSP00000262829.7:p.Ala343Ser
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.1024G>T
  hgvsp: ENSP00000380470.2:p.Ala342Ser
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1093G>T
  hgvsp: ENSP00000391670.2:p.Ala365Ser
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3445
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31925
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala436Ser
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD

22-36141975-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36141975
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36141975
    reference: chr 22
allele count: 8
allele frequency: 6.596197292261011e-5
allele num: 121282
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1093G>A
  hgvsp: ENSP00000391670.2:p.Ala365Thr
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.1027G>A
  hgvsp: ENSP00000262829.7:p.Ala343Thr
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1306G>A
  hgvsp: ENSP00000413035.2:p.Ala436Thr
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.642G>A
  hgvsp: ENSP00000474464.1:p.Ala215Thr
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2228G>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1081G>A
  hgvsp: ENSP00000405651.2:p.Ala361Thr
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1044G>A
  hgvsp: ENST00000405409.2:c.1044G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1053G>A
  hgvsp: ENST00000414461.2:c.1053G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.1024G>A
  hgvsp: ENSP00000380470.2:p.Ala342Thr
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1053G>A
  hgvsp: ENST00000359369.4:c.1053G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31925
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3445
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala436Thr
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS

22-36141976-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36141976
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36141976
    reference: chr 22
allele count: 2
allele frequency: 1.648967746190884e-5
allele num: 121288
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1092C>T
  hgvsp: ENST00000449924.2:c.1092C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1080C>T
  hgvsp: ENST00000416721.2:c.1080C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1305C>T
  hgvsp: ENST00000438146.2:c.1305C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1052C>T
  hgvsp: ENSP00000407855.2:p.Ala351Val
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.641C>T
  hgvsp: ENST00000495377.2:c.641C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1043C>T
  hgvsp: ENSP00000384944.2:p.Ala348Val
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2227C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1052C>T
  hgvsp: ENSP00000352328.4:p.Ala351Val
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.1026C>T
  hgvsp: ENST00000262829.7:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.1023C>T
  hgvsp: ENST00000397303.2:c.1023C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3445
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31922
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2778
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala351Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

22-36141994-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36141994
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36141994
    reference: chr 22
allele count: 7
allele frequency: 5.771196781321109e-5
allele num: 121292
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1287C>T
  hgvsp: ENST00000438146.2:c.1287C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1074C>T
  hgvsp: ENST00000449924.2:c.1074C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.1005C>T
  hgvsp: ENST00000397303.2:c.1005C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2209C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1034C>T
  hgvsp: ENSP00000352328.4:p.Pro345Leu
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1034C>T
  hgvsp: ENSP00000407855.2:p.Pro345Leu
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1062C>T
  hgvsp: ENST00000416721.2:c.1062C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.623C>T
  hgvsp: ENST00000495377.2:c.623C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1025C>T
  hgvsp: ENSP00000384944.2:p.Pro342Leu
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.1008C>T
  hgvsp: ENST00000262829.7:c.1008C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1549
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3449
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2778
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3445
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31922
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro345Leu
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

22-36142007-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36142007
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36142007
    reference: chr 22
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1274C>G
  hgvsp: ENSP00000413035.2:p.Ala425Gly
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1061C>G
  hgvsp: ENSP00000391670.2:p.Ala354Gly
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1012C>G
  hgvsp: ENSP00000384944.2:p.Pro338Ala
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1021C>G
  hgvsp: ENSP00000352328.4:p.Pro341Ala
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.995C>G
  hgvsp: ENSP00000262829.7:p.Ala332Gly
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1049C>G
  hgvsp: ENSP00000405651.2:p.Ala350Gly
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1021C>G
  hgvsp: ENSP00000407855.2:p.Pro341Ala
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.992C>G
  hgvsp: ENSP00000380470.2:p.Ala331Gly
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2196C>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.610C>G
  hgvsp: ENSP00000474464.1:p.Ala204Gly
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3445
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3412
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31921
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala425Gly
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

22-36142017-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36142017
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36142017
    reference: chr 22
allele count: 3
allele frequency: 2.473614775725594e-5
allele num: 121280
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1264C>T
  hgvsp: ENSP00000413035.2:p.Pro422Ser
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1039C>T
  hgvsp: ENSP00000405651.2:p.Pro347Ser
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1051C>T
  hgvsp: ENSP00000391670.2:p.Pro351Ser
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2186C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.985C>T
  hgvsp: ENSP00000262829.7:p.Pro329Ser
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.600C>T
  hgvsp: ENSP00000474464.1:p.Pro201Ser
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1011C>T
  hgvsp: ENST00000359369.4:c.1011C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1011C>T
  hgvsp: ENST00000414461.2:c.1011C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.982C>T
  hgvsp: ENSP00000380470.2:p.Pro328Ser
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.1002C>T
  hgvsp: ENST00000405409.2:c.1002C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3337
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31920
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3445
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro422Ser
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

22-36142020-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36142020
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36142020
    reference: chr 22
allele count: 1
allele frequency: 8.246470510621453e-6
allele num: 121264
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.979G>A
  hgvsp: ENSP00000380470.2:p.Asp327Asn
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1008G>A
  hgvsp: ENST00000359369.4:c.1008G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1036G>A
  hgvsp: ENSP00000405651.2:p.Asp346Asn
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.999G>A
  hgvsp: ENST00000405409.2:c.999G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1261G>A
  hgvsp: ENSP00000413035.2:p.Asp421Asn
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.597G>A
  hgvsp: ENSP00000474464.1:p.Asp200Asn
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.982G>A
  hgvsp: ENSP00000262829.7:p.Asp328Asn
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1048G>A
  hgvsp: ENSP00000391670.2:p.Asp350Asn
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2183G>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1008G>A
  hgvsp: ENST00000414461.2:c.1008G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3325
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3445
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31919
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp421Asn
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/22-36142023-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36142023
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36142023
    reference: chr 22
allele count: 1
allele frequency: 8.246878556466378e-6
allele num: 121258
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.979G>T
  hgvsp: ENSP00000262829.7:p.Ala327Ser
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1258G>T
  hgvsp: ENSP00000413035.2:p.Ala420Ser
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1045G>T
  hgvsp: ENSP00000391670.2:p.Ala349Ser
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.594G>T
  hgvsp: ENSP00000474464.1:p.Ala199Ser
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.996G>T
  hgvsp: ENSP00000384944.2:p.Gln332His
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1005G>T
  hgvsp: ENSP00000407855.2:p.Gln335His
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1033G>T
  hgvsp: ENSP00000405651.2:p.Ala345Ser
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.976G>T
  hgvsp: ENSP00000380470.2:p.Ala326Ser
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1005G>T
  hgvsp: ENSP00000352328.4:p.Gln335His
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2180G>T
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3411
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31919
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3444
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 714
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala420Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

22-36142026-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36142026
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36142026
    reference: chr 22
allele count: 1
allele frequency: 8.248375070111188e-6
allele num: 121236
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2177A>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.973A>C
  hgvsp: ENSP00000380470.2:p.Thr325Pro
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.976A>C
  hgvsp: ENSP00000262829.7:p.Thr326Pro
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1002A>C
  hgvsp: ENST00000359369.4:c.1002A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1030A>C
  hgvsp: ENSP00000405651.2:p.Thr344Pro
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1255A>C
  hgvsp: ENSP00000413035.2:p.Thr419Pro
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.591A>C
  hgvsp: ENSP00000474464.1:p.Thr198Pro
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1002A>C
  hgvsp: ENST00000414461.2:c.1002A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1042A>C
  hgvsp: ENSP00000391670.2:p.Thr348Pro
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.993A>C
  hgvsp: ENST00000405409.2:c.993A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3444
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31918
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Thr419Pro
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

22-36142027-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36142027
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36142027
    reference: chr 22
allele count: 3
allele frequency: 2.474675817467912e-5
allele num: 121228
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.590C>A
  hgvsp: ENSP00000474464.1:p.Tyr197Ter
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1254C>A
  hgvsp: ENSP00000413035.2:p.Tyr418Ter
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.972C>A
  hgvsp: ENSP00000380470.2:p.Tyr324Ter
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2176C>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.1001C>A
  hgvsp: ENSP00000407855.2:p.Thr334Lys
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.1001C>A
  hgvsp: ENSP00000352328.4:p.Thr334Lys
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1029C>A
  hgvsp: ENSP00000405651.2:p.Tyr343Ter
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.975C>A
  hgvsp: ENSP00000262829.7:p.Tyr325Ter
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1041C>A
  hgvsp: ENSP00000391670.2:p.Tyr347Ter
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.992C>A
  hgvsp: ENSP00000384944.2:p.Thr331Lys
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3444
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1525
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31918
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Tyr418Ter
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
reference allele: G
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/22-36142029-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36142029
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36142029
    reference: chr 22
allele count: 1
allele frequency: 8.249872126982032e-6
allele num: 121214
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.973T>G
  hgvsp: ENSP00000262829.7:p.Tyr325Asp
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.999T>G
  hgvsp: ENSP00000407855.2:p.Cys333Trp
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1252T>G
  hgvsp: ENSP00000413035.2:p.Tyr418Asp
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.588T>G
  hgvsp: ENSP00000474464.1:p.Tyr197Asp
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.990T>G
  hgvsp: ENSP00000384944.2:p.Cys330Trp
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.999T>G
  hgvsp: ENSP00000352328.4:p.Cys333Trp
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1039T>G
  hgvsp: ENSP00000391670.2:p.Tyr347Asp
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2174T>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.970T>G
  hgvsp: ENSP00000380470.2:p.Tyr324Asp
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1027T>G
  hgvsp: ENSP00000405651.2:p.Tyr343Asp
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31917
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3385
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3446
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Tyr418Asp
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/22-36142031-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36142031
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36142031
    reference: chr 22
allele count: 5348
allele frequency: 4.513461051565533e-2
allele num: 118490
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1037T>G
  hgvsp: ENSP00000391670.2:p.Val346Gly
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.988T>G
  hgvsp: ENSP00000384944.2:p.Cys330Gly
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.997T>G
  hgvsp: ENSP00000352328.4:p.Cys333Gly
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1250T>G
  hgvsp: ENSP00000413035.2:p.Val417Gly
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1025T>G
  hgvsp: ENSP00000405651.2:p.Val342Gly
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.968T>G
  hgvsp: ENSP00000380470.2:p.Val323Gly
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.586T>G
  hgvsp: ENSP00000474464.1:p.Val196Gly
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.971T>G
  hgvsp: ENSP00000262829.7:p.Val324Gly
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2172T>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.997T>G
  hgvsp: ENSP00000407855.2:p.Cys333Gly
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 1480
  bin: 6.75e1
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 5.75e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 2812
  bin: 8.25e1
  variant carriers: 122
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 4.75e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 3172
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 3159
  bin: 8.75e1
  variant carriers: 107
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 5.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 6.25e1
  variant carriers: 96
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 3.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 32437
  bin: 9.75e1
  variant carriers: 4482
genotype depth: GenotypeDepth
  all individuals: 3105
  bin: 2.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 3.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 2230
  bin: 7.75e1
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 7.25e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 3460
  bin: 9.25e1
  variant carriers: 89
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 7.25e1
  variant carriers: 35
hgvs: p.Val417Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/22-36142032-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36142032
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36142032
    reference: chr 22
allele count: 1
allele frequency: 8.25000825000825e-6
allele num: 121212
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1036G>T
  hgvsp: ENSP00000391670.2:p.Val346Leu
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.996G>T
  hgvsp: ENST00000414461.2:c.996G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.970G>T
  hgvsp: ENSP00000262829.7:p.Val324Leu
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.996G>T
  hgvsp: ENST00000359369.4:c.996G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.585G>T
  hgvsp: ENSP00000474464.1:p.Val196Leu
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.967G>T
  hgvsp: ENSP00000380470.2:p.Val323Leu
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1249G>T
  hgvsp: ENSP00000413035.2:p.Val417Leu
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2171G>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1024G>T
  hgvsp: ENSP00000405651.2:p.Val342Leu
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.987G>T
  hgvsp: ENST00000405409.2:c.987G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3337
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2897
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3614
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3202
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30990
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3261
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val417Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

22-36142032-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36142032
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36142032
    reference: chr 22
allele count: 1
allele frequency: 8.25000825000825e-6
allele num: 121212
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.996G>A
  hgvsp: ENST00000359369.4:c.996G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1249G>A
  hgvsp: ENSP00000413035.2:p.Val417Met
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1024G>A
  hgvsp: ENSP00000405651.2:p.Val342Met
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.585G>A
  hgvsp: ENSP00000474464.1:p.Val196Met
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.967G>A
  hgvsp: ENSP00000380470.2:p.Val323Met
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2171G>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1036G>A
  hgvsp: ENSP00000391670.2:p.Val346Met
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.970G>A
  hgvsp: ENSP00000262829.7:p.Val324Met
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.996G>A
  hgvsp: ENST00000414461.2:c.996G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.987G>A
  hgvsp: ENST00000405409.2:c.987G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3337
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2897
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3261
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3202
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3614
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30990
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val417Met
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

22-36142039-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36142039
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36142039
    reference: chr 22
allele count: 8
allele frequency: 6.601858423146116e-5
allele num: 121178
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.578T>C
  hgvsp: ENST00000495377.2:c.578T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.989T>C
  hgvsp: ENSP00000352328.4:p.Met330Thr
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.960T>C
  hgvsp: ENST00000397303.2:c.960T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2164T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1242T>C
  hgvsp: ENST00000438146.2:c.1242T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.989T>C
  hgvsp: ENSP00000407855.2:p.Met330Thr
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1029T>C
  hgvsp: ENST00000449924.2:c.1029T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1017T>C
  hgvsp: ENST00000416721.2:c.1017T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.980T>C
  hgvsp: ENSP00000384944.2:p.Met327Thr
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.963T>C
  hgvsp: ENST00000262829.7:c.963T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30989
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3195
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3262
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3613
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2897
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Met330Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/22-36142042-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36142042
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36142042
    reference: chr 22
allele count: 1
allele frequency: 8.252731654177533e-6
allele num: 121172
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.986T>G
  hgvsp: ENSP00000352328.4:p.Val329Gly
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2161T>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.977T>G
  hgvsp: ENSP00000384944.2:p.Val326Gly
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1239T>G
  hgvsp: ENST00000438146.2:c.1239T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.986T>G
  hgvsp: ENSP00000407855.2:p.Val329Gly
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1014T>G
  hgvsp: ENST00000416721.2:c.1014T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.575T>G
  hgvsp: ENST00000495377.2:c.575T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1026T>G
  hgvsp: ENST00000449924.2:c.1026T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.960T>G
  hgvsp: ENST00000262829.7:c.960T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.957T>G
  hgvsp: ENST00000397303.2:c.957T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9906
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3262
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3278
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30987
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3613
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val329Gly
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

22-36142054-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36142054
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36142054
    reference: chr 22
allele count: 1
allele frequency: 8.259002312520648e-6
allele num: 121080
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.575-12T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.957-12T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.986-12T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1239-12T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.960-12T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.986-12T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.977-12T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1014-12T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1026-12T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2161-12T>C
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3613
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2985
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30988
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3260
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

22-36142065-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36142065
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36142065
    reference: chr 22
allele count: 1
allele frequency: 8.272119647938589e-6
allele num: 120888
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.986-23C>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2161-23C>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1014-23C>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.960-23C>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.977-23C>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.575-23C>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1026-23C>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.957-23C>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.986-23C>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1239-23C>A
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3261
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3613
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30986
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

22-36142072-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36142072
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36142072
    reference: chr 22
allele count: 1
allele frequency: 8.27417299640901e-6
allele num: 120858
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.575-30T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1014-30T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.986-30T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.957-30T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.977-30T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.960-30T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1239-30T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1026-30T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2161-30T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.986-30T>C
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3261
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3613
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30986
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1264
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

22-36142076-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36142076
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36142076
    reference: chr 22
allele count: 546
allele frequency: 4.519568240513873e-3
allele num: 120808
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.575-34T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.977-34T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1014-34T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1026-34T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2161-34T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.986-34T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.986-34T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.960-34T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.957-34T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1239-34T>C
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2549
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3261
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2064
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30978
  bin: 9.75e1
  variant carriers: 471
genotype depth: GenotypeDepth
  all individuals: 3620
  bin: 9.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 8
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

22-36142079-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36142079
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36142079
    reference: chr 22
allele count: 1
allele frequency: 8.279105194310599e-6
allele num: 120786
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.960-37T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.957-37T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1239-37T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.986-37T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.986-37T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.575-37T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1026-37T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1014-37T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2161-37T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.977-37T>C
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3648
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2387
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30818
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 605
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 707
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

22-36142080-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36142080
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36142080
    reference: chr 22
allele count: 1
allele frequency: 8.283357078956959e-6
allele num: 120724
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.977-38C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.575-38C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1239-38C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.986-38C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.960-38C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.986-38C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2161-38C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1026-38C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.957-38C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1014-38C>T
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30818
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3648
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50551
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

22-36142087-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36142087
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36142087
    reference: chr 22
allele count: 1
allele frequency: 8.301097405076952e-6
allele num: 120466
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.977-45T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.986-45T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1026-45T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.957-45T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.960-45T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2161-45T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.986-45T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1239-45T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1014-45T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.575-45T>C
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30818
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3648
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

22-36142089-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36142089
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36142089
    reference: chr 22
allele count: 1
allele frequency: 8.307993951780402e-6
allele num: 120366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1014-47G>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1239-47G>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.960-47G>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.977-47G>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.986-47G>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.575-47G>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1026-47G>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2161-47G>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.957-47G>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.986-47G>A
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3649
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1741
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30817
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2157
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

22-36142090-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36142090
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36142090
    reference: chr 22
allele count: 1
allele frequency: 8.31255195344971e-6
allele num: 120300
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.986-48A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.957-48A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1014-48A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.986-48A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.960-48A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1239-48A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.977-48A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.575-48A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2161-48A>G
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1026-48A>G
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3649
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2527
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1731
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30817
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 734
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

22-36142090-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36142090
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36142091
    reference: chr 22
allele count: 1
allele frequency: 8.31255195344971e-6
allele num: 120300
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1026-49dupT
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.575-49dupT
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.977-49dupT
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1239-49dupT
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1014-49dupT
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.957-49dupT
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.986-49dupT
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2161-49dupT
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.960-49dupT
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.986-49dupT
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2527
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3649
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1731
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30817
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 869
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

22-36142091-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36142091
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36142091
    reference: chr 22
allele count: 15
allele frequency: 1.246385482101905e-4
allele num: 120348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.957-49T>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.986-49T>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.977-49T>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1239-49T>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1026-49T>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2161-49T>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.986-49T>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.575-49T>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1014-49T>A
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.960-49T>A
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3287
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1721
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30817
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3649
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50555
  bin: 9.75e1
  variant carriers: 15
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

22-36142092-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36142092
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36142092
    reference: chr 22
allele count: 1
allele frequency: 8.307027745472669e-6
allele num: 120380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.960-50T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.986-50T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.986-50T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1014-50T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.977-50T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2161-50T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1026-50T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.957-50T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1239-50T>C
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.575-50T>C
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3287
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2541
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30815
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3651
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

22-36142472-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36142472
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 36142472
    reference: chr 22
allele count: 1
allele frequency: 8.787191789247992e-6
allele num: 113802
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000384944
  ensembl transcript: ENST00000405409
  gene symbol: RBFOX2
  hgvsc: ENST00000405409.2:c.976+48C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000352328
  ensembl transcript: ENST00000359369
  gene symbol: RBFOX2
  hgvsc: ENST00000359369.4:c.985+48C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl transcript: ENST00000463509
  gene symbol: RBFOX2
  hgvsc: ENST00000463509.1:n.2160+48C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000413035
  ensembl transcript: ENST00000438146
  gene symbol: RBFOX2
  hgvsc: ENST00000438146.2:c.1238+48C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000391670
  ensembl transcript: ENST00000449924
  gene symbol: RBFOX2
  hgvsc: ENST00000449924.2:c.1025+48C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000262829
  ensembl transcript: ENST00000262829
  gene symbol: RBFOX2
  hgvsc: ENST00000262829.7:c.959+48C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000474464
  ensembl transcript: ENST00000495377
  gene symbol: RBFOX2
  hgvsc: ENST00000495377.2:c.574+48C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000380470
  ensembl transcript: ENST00000397303
  gene symbol: RBFOX2
  hgvsc: ENST00000397303.2:c.956+48C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000407855
  ensembl transcript: ENST00000414461
  gene symbol: RBFOX2
  hgvsc: ENST00000414461.2:c.985+48C>T
  variant of: http://identifiers.org/hgnc/9906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100320
  ensembl protein: ENSP00000405651
  ensembl transcript: ENST00000416721
  gene symbol: RBFOX2
  hgvsc: ENST00000416721.2:c.1013+48C>T
  variant of: http://identifiers.org/hgnc/9906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2953
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: G

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8114
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9736
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.07e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.239e0

MQ
type: SiteQuality
SIO_000300: 5.903e1

VQSLOD
type: SiteQuality
SIO_000300: -1.514e-1

QD
type: SiteQuality
SIO_000300: 1.356e1

FS
type: SiteQuality
SIO_000300: 4.525e0

DP
type: SiteQuality
SIO_000300: 1.311027e6

African
type: Population
allele count: 6
allele frequency: 6.197066721751704e-4
allele num: 9682
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.209757663296421e-5
allele num: 62310
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11032
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12274
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.53e0

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.37e-1

QD
type: SiteQuality
SIO_000300: 1.257e1

DP
type: SiteQuality
SIO_000300: 1.286627e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.96e-1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9622
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6020
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10990
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.59e0

DP
type: SiteQuality
SIO_000300: 1.272231e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.08e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.904e1

MQRankSum
type: SiteQuality
SIO_000300: -1.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.88e-1

QD
type: SiteQuality
SIO_000300: 1.36e1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61296
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11704
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e0

MQRankSum
type: SiteQuality
SIO_000300: 1.33e-1

QD
type: SiteQuality
SIO_000300: 1.818e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.254872e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.56e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -4.061e-1

GenotypeQuality
all individuals: 936
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2016
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1388
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4602
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 778
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 857
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6300
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15174
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.563574957783476e-5
allele num: 63956
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10876
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9902
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.723e1

VQSLOD
type: SiteQuality
SIO_000300: -2.305e0

QD
type: SiteQuality
SIO_000300: 1.185e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.308609e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e0

MQRankSum
type: SiteQuality
SIO_000300: -1.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.395e0

GenotypeQuality
all individuals: 123
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4375
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 946
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2458
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1793
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4497
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1945
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3859
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1388
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 30034
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10938
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.556904873112253e-5
allele num: 64230
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6324
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9922
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.959247648902821e-4
allele num: 15312
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8394
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.28e0

QD
type: SiteQuality
SIO_000300: 1.731e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -6.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.7e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.346e0

DP
type: SiteQuality
SIO_000300: 1.328873e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e0

GenotypeQuality
all individuals: 1712
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1513
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 877
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4530
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 1.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10968
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15352
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8420
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.553711817532084e-5
allele num: 64362
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9938
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6318
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.376908e6

MQRankSum
type: SiteQuality
SIO_000300: -1.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.01e-2

QD
type: SiteQuality
SIO_000300: 1.522e1

VQSLOD
type: SiteQuality
SIO_000300: 7.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.62e-1

FS
type: SiteQuality
SIO_000300: 3.854e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.552e0

GenotypeQuality
all individuals: 2710
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4594
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1567
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3111
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 880
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1322
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1162
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2679
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1382
bin: 9.75e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.649576888503146e-5
allele num: 64522
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10982
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6332
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15416
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9956
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.397022e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.708e0

MQRankSum
type: SiteQuality
SIO_000300: 1.2e-2

FS
type: SiteQuality
SIO_000300: 2.504e0

MQ
type: SiteQuality
SIO_000300: 5.909e1

QD
type: SiteQuality
SIO_000300: 1.226e1

GenotypeQuality
all individuals: 759
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 943
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2327
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1476
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4681
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 900
bin: 7.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6342
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11008
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9966
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64598
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8442
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.469142191745374e-5
allele num: 15458
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -5.62e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.62e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

FS
type: SiteQuality
SIO_000300: 1.494e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.21e0

MQ
type: SiteQuality
SIO_000300: 5.906e1

DP
type: SiteQuality
SIO_000300: 1.406844e6

QD
type: SiteQuality
SIO_000300: 1.059e1

GenotypeQuality
all individuals: 867
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1863
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 745
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4633
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1375
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 158
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2085
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1342
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11028
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6350
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9970
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8472
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.546120782955564e-5
allele num: 64678
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.426777e6

VQSLOD
type: SiteQuality
SIO_000300: -3.604e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.15e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

QD
type: SiteQuality
SIO_000300: 3.28e0

FS
type: SiteQuality
SIO_000300: 5.37e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.3e-2

MQ
type: SiteQuality
SIO_000300: 5.997e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8472
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6350
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15460
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.067827348567283e-5
allele num: 11028
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9970
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64678
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.997e1

DP
type: SiteQuality
SIO_000300: 1.426777e6

QD
type: SiteQuality
SIO_000300: 3.28e0

VQSLOD
type: SiteQuality
SIO_000300: -3.604e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.3e-2

FS
type: SiteQuality
SIO_000300: 5.37e0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2013
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64664
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8466
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11028
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.00341159943809e-4
allele num: 9966
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.476683937823834e-5
allele num: 15440
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6362
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.176e0

MQRankSum
type: SiteQuality
SIO_000300: 1.48e0

DP
type: SiteQuality
SIO_000300: 1.431807e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.9e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.905e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

QD
type: SiteQuality
SIO_000300: 1.468e1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 8

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8498
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9994
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.232209968578646e-4
allele num: 64924
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6366
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11072
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.444123e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.123e0

VQSLOD
type: SiteQuality
SIO_000300: 1.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

FS
type: SiteQuality
SIO_000300: 8.234e0

QD
type: SiteQuality
SIO_000300: 1.172e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.46e-1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 54
bin: 7.5e0
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.988014382740711e-5
allele num: 10012
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11074
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64974
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15544
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.109e0

FS
type: SiteQuality
SIO_000300: 1.594e0

VQSLOD
type: SiteQuality
SIO_000300: 4.83e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.461e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.23e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

DP
type: SiteQuality
SIO_000300: 1.449931e6

MQRankSum
type: SiteQuality
SIO_000300: 5.620000000000001e-1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10022
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65086
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.411900487304436e-5
allele num: 15596
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11096
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.77e-1

MQ
type: SiteQuality
SIO_000300: 5.903e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

DP
type: SiteQuality
SIO_000300: 1.460228e6

VQSLOD
type: SiteQuality
SIO_000300: 2.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.56e0

QD
type: SiteQuality
SIO_000300: 8.35e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.96e-1

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10034
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15640
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11114
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6392
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.534024667116647e-5
allele num: 65188
num of homozygotes: 0

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

Other
type: Population
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allele num: 886
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MQRankSum
type: SiteQuality
SIO_000300: 5.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.22e-1

QD
type: SiteQuality
SIO_000300: 1.433e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.93e-1

DP
type: SiteQuality
SIO_000300: 1.470515e6

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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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11164
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6416
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African
type: Population
allele count: 1
allele frequency: 9.908838684106223e-5
allele num: 10092
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Other
type: Population
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 65472
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ReadPosRankSum
type: SiteQuality
SIO_000300: -3.86e-1

MQ
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
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MQRankSum
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 5.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.55e-1

DP
type: SiteQuality
SIO_000300: 1.48771e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11212
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10122
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523739867129884e-5
allele num: 65628
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6440
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele num: 888
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.138e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -3.37e-2

ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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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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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 353
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 791
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 2.960915909988156e-4
allele num: 10132
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11212
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15784
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65666
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.08e0

QD
type: SiteQuality
SIO_000300: 1.127e1

FS
type: SiteQuality
SIO_000300: 1.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.73e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.50081e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.28e-1

GenotypeQuality
all individuals: 203
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 6

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

GenotypeQuality
all individuals: 364
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 791
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11212
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15784
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 4.934859849980261e-4
allele num: 10132
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.522858100082234e-5
allele num: 65666
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.127e1

FS
type: SiteQuality
SIO_000300: 1.75e0

VQSLOD
type: SiteQuality
SIO_000300: 2.08e0

DP
type: SiteQuality
SIO_000300: 1.50081e6

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.73e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.28e-1

GenotypeQuality
all individuals: 207
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
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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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GenotypeQuality
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GenotypeQuality
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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
all individuals: 779
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10130
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 7.012622720897616e-4
allele num: 8556
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.327512022272843e-5
allele num: 15804
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11218
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65640
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6440
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.24e-1

QD
type: SiteQuality
SIO_000300: 9.35e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.600000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.3e-2

DP
type: SiteQuality
SIO_000300: 1.501646e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.463e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.51e-1

GenotypeQuality
all individuals: 135
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 7.5e0
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GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 228
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variant carriers: 0

GenotypeQuality
all individuals: 10
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 10

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5005
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11242
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6456
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65650
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 11
allele frequency: 6.95586189452384e-4
allele num: 15814
num of homozygotes: 1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.53e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.55e-1

DP
type: SiteQuality
SIO_000300: 1.507368e6

FS
type: SiteQuality
SIO_000300: 3.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.478e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.39e-1

GenotypeQuality
all individuals: 4753
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 269
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variant carriers: 0

GenotypeQuality
all individuals: 327
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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: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4531
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GenotypeQuality
all individuals: 45896
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.555597038143239e-5
allele num: 64284
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15448
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9882
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6306
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11008
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -7.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 7.5e0

FS
type: SiteQuality
SIO_000300: 3.11e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.587e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.03e0

VQSLOD
type: SiteQuality
SIO_000300: -1.131e0

DP
type: SiteQuality
SIO_000300: 1.471717e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.29e-1

GenotypeDepth
all individuals: 61
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1283
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 649
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.06951871657754e-4
allele num: 9350
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6036
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61196
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14860
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.11e0

VQSLOD
type: SiteQuality
SIO_000300: -2.832e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -6.67e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.380885e6

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19601
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5526
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.284382284382284e-5
allele num: 13728
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54456
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 760
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9312
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7194
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.15e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.135e0

QD
type: SiteQuality
SIO_000300: 6.96e0

DP
type: SiteQuality
SIO_000300: 1.096623e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.36e-1

MQ
type: SiteQuality
SIO_000300: 6.074e1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 444
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.836344939033348e-5
allele num: 54456
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9312
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8370
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5526
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7194
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 760
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.135e0

DP
type: SiteQuality
SIO_000300: 1.096623e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.34e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.45e0

MQRankSum
type: SiteQuality
SIO_000300: 8.25e-1

MQ
type: SiteQuality
SIO_000300: 6.074e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 6.96e0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
all individuals: 206
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GenotypeQuality
all individuals: 669
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8740
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7890
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.954346466541588e-5
allele num: 51168
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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5272
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.45715e5

VQSLOD
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FS
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SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: -4.9e-3

MQRankSum
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QD
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MQ
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ReadPosRankSum
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 8.99e-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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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 12952
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 50452
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 8658
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5228
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.286670097786928e-4
allele num: 7772
num of homozygotes: 0

Other
type: Population
allele count: 0
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allele num: 726
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.0446e1

DP
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VQSLOD
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QD
type: SiteQuality
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ClippingRankSum
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SIO_000300: -8.0e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: -5.3e-3

ReadPosRankSum
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SIO_000300: 4.0e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 686
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8198
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5040
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.087682672233821e-5
allele num: 47900
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.69e-1

QD
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BaseQRankSum
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SIO_000300: 2.15e0

InbreedingCoeff
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SIO_000300: -7.900000000000001e-3

DP
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MQ
type: SiteQuality
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VQSLOD
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ReadPosRankSum
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SIO_000300: 1.66e0

FS
type: SiteQuality
SIO_000300: 4.036e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.655e0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4990
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.201327619527771e-5
allele num: 47604
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7300
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8146
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12396
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.117e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.32e0

QD
type: SiteQuality
SIO_000300: 1.34e1

DP
type: SiteQuality
SIO_000300: 8.69205e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e0

MQRankSum
type: SiteQuality
SIO_000300: -4.69e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4920
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46228
num of homozygotes: 0

South Asian
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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: 6072
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.406469760900141e-4
allele num: 7110
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 5.07e-1

InbreedingCoeff
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FS
type: SiteQuality
SIO_000300: 2.144e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.909999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.48e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.216e1

BaseQRankSum
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SIO_000300: -2.652e0

MQRankSum
type: SiteQuality
SIO_000300: 1.77e-1

DP
type: SiteQuality
SIO_000300: 8.54947e5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 1
allele frequency: 1.421666192777936e-4
allele num: 7034
num of homozygotes: 0

Latino
type: Population
allele count: 1
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allele num: 7804
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Other
type: Population
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allele frequency: 0.0e0
allele num: 658
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.588e1

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

East Asian
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allele frequency: 1.646903820816864e-4
allele num: 6072
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4894
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 45806
num of homozygotes: 0

Latino
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South Asian
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Other
type: Population
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num of homozygotes: 0

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
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DP
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InbreedingCoeff
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QD
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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SIO_000300: 9.22e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
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Latino
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allele frequency: 5.763688760806917e-4
allele num: 6940
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East Asian
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African
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allele frequency: 1.590330788804071e-4
allele num: 6288
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European (Finnish)
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.438310738320491e-5
allele num: 41012
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South Asian
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BaseQRankSum
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VQSLOD
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MQRankSum
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DP
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FS
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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MQ
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 50542
bin: 9.75e1
variant carriers: 340

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.217730150998539e-4
allele num: 16424
num of homozygotes: 0

African
type: Population
allele count: 316
allele frequency: 3.046664095642113e-2
allele num: 10372
num of homozygotes: 4

Latino
type: Population
allele count: 15
allele frequency: 1.295560545862843e-3
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.202212070209185e-4
allele num: 66544
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.023888720895071e-4
allele num: 6614
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

FS
type: SiteQuality
SIO_000300: 2.062e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.42e-2

MQ
type: SiteQuality
SIO_000300: 5.97e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.488e0

VQSLOD
type: SiteQuality
SIO_000300: 4.05e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.39e-1

QD
type: SiteQuality
SIO_000300: 1.433e1

DP
type: SiteQuality
SIO_000300: 5.795429e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.23e-1

GenotypeQuality
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bin: 3.75e1
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
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bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50253929140247e-5
allele num: 66554
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.05e-1

DP
type: SiteQuality
SIO_000300: 5.770674e6

VQSLOD
type: SiteQuality
SIO_000300: -1.351e0

ClippingRankSum
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SIO_000300: 5.48e-1

FS
type: SiteQuality
SIO_000300: 3.397e0

InbreedingCoeff
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SIO_000300: 1.17e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 9.449999999999999e0

MQ
type: SiteQuality
SIO_000300: 5.984e1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e0

QD
type: SiteQuality
SIO_000300: 1.634e1

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66556
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.63948332369385e-5
allele num: 10374
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.944e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.11e0

DP
type: SiteQuality
SIO_000300: 5.771881e6

MQRankSum
type: SiteQuality
SIO_000300: 6.19e-1

QD
type: SiteQuality
SIO_000300: 2.56e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.03e-2

FS
type: SiteQuality
SIO_000300: 2.203e0

VQSLOD
type: SiteQuality
SIO_000300: -3.473e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.77e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.003e0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.822600243013366e-4
allele num: 16460
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.512696457012351e-5
allele num: 66554
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -5.45e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.66e-1

FS
type: SiteQuality
SIO_000300: 7.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.79e0

MQ
type: SiteQuality
SIO_000300: 5.978e1

QD
type: SiteQuality
SIO_000300: 1.577e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.2e-3

DP
type: SiteQuality
SIO_000300: 5.773295e6

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 47
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66554
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.632e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.17e0

DP
type: SiteQuality
SIO_000300: 5.772753e6

MQRankSum
type: SiteQuality
SIO_000300: -2.83e-1

FS
type: SiteQuality
SIO_000300: 2.887e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.733e0

GenotypeQuality
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16470
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502268425322237e-5
allele num: 66566
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 5.903e1

FS
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 5.773781e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e0

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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variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501185936890143e-5
allele num: 66614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: 7.76e0

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

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

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

Other
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South Asian
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allele frequency: 6.05766900896535e-5
allele num: 16508
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European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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VQSLOD
type: SiteQuality
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FS
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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DP
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BaseQRankSum
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MQ
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QD
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GenotypeQuality
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variant carriers: 8

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8.75e1
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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: 25
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

South Asian
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allele count: 7
allele frequency: 4.240368306275745e-4
allele num: 16508
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

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

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

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

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

DP
type: SiteQuality
SIO_000300: 5.778134e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.639e0

VQSLOD
type: SiteQuality
SIO_000300: 8.38e-1

MQ
type: SiteQuality
SIO_000300: 5.955e1

MQRankSum
type: SiteQuality
SIO_000300: -1.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.48e-1

QD
type: SiteQuality
SIO_000300: 1.197e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 5.37e-1

GenotypeQuality
all individuals: 439
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 7.5e0
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GenotypeQuality
all individuals: 720
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1576
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.001110410852015e-5
allele num: 66642
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -5.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.959e1

QD
type: SiteQuality
SIO_000300: 1.165e1

VQSLOD
type: SiteQuality
SIO_000300: 9.56e-1

FS
type: SiteQuality
SIO_000300: 1.12e0

MQRankSum
type: SiteQuality
SIO_000300: 4.72e-1

DP
type: SiteQuality
SIO_000300: 5.776975e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.25e-1

GenotypeQuality
all individuals: 720
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1570
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variant carriers: 0

GenotypeQuality
all individuals: 12
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GenotypeQuality
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GenotypeQuality
all individuals: 37
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
all individuals: 439
bin: 9.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.05026256564141e-4
allele num: 66650
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 5.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.138e1

DP
type: SiteQuality
SIO_000300: 5.777218e6

VQSLOD
type: SiteQuality
SIO_000300: 2.31e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.12e0

MQRankSum
type: SiteQuality
SIO_000300: 5.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.47e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

GenotypeQuality
all individuals: 47
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 719
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GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 0
bin: 2.5e0
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GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
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variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 509
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variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1572
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50469
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 439
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5865
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500195025353296e-5
allele num: 66658
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.452e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 9.13e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.54e-1

DP
type: SiteQuality
SIO_000300: 5.775282e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.17e-1

QD
type: SiteQuality
SIO_000300: 1.134e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.54e-1

GenotypeQuality
all individuals: 34
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5822
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variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 56
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variant carriers: 0

GenotypeQuality
all individuals: 17
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GenotypeQuality
all individuals: 51
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GenotypeQuality
all individuals: 1569
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 2.25e1
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GenotypeQuality
all individuals: 50467
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 508
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variant carriers: 0

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

GenotypeQuality
all individuals: 719
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 9.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.500990217847926e-5
allele num: 66652
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 6.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.98e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.8e-1

DP
type: SiteQuality
SIO_000300: 5.774882e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.158e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.82e-1

GenotypeQuality
all individuals: 30
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variant carriers: 0

GenotypeQuality
all individuals: 63
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 23
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 715
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variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 9.25e1
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GenotypeQuality
all individuals: 50464
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500420117632937e-5
allele num: 66648
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -6.860000000000001e-1

FS
type: SiteQuality
SIO_000300: 4.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.97e0

DP
type: SiteQuality
SIO_000300: 5.774141e6

MQ
type: SiteQuality
SIO_000300: 5.981e1

VQSLOD
type: SiteQuality
SIO_000300: -1.673e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.84e0

QD
type: SiteQuality
SIO_000300: 6.29e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.033e0

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: 1562
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GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500555205426008e-5
allele num: 66642
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -3.017e0

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.580000000000001e-1

DP
type: SiteQuality
SIO_000300: 5.77344e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.91e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -1.774e0

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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bin: 6.75e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500555205426008e-5
allele num: 66642
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.87e-1

MQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.024e0

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 5.772802e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQ
type: SiteQuality
SIO_000300: 5.973e1

FS
type: SiteQuality
SIO_000300: 2.6e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.03e-1

GenotypeQuality
all individuals: 290
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50463
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 702
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5707
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 437
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 504
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1549
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 59
bin: 3.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.501665616278023e-5
allele num: 66642
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 5.21e0

MQ
type: SiteQuality
SIO_000300: 5.919e1

FS
type: SiteQuality
SIO_000300: 2.623e0

VQSLOD
type: SiteQuality
SIO_000300: -2.776e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.479e0

DP
type: SiteQuality
SIO_000300: 5.772484e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 7.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.52e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.216e0

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

GenotypeQuality
all individuals: 90
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5625
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
all individuals: 690
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
all individuals: 286
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GenotypeQuality
all individuals: 50464
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variant carriers: 1

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

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1519
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 8.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.67305088024763e-5
allele num: 10338
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66634
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -1.189e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.46e-1

FS
type: SiteQuality
SIO_000300: 1.0193e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.176e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

DP
type: SiteQuality
SIO_000300: 5.772094e6

MQRankSum
type: SiteQuality
SIO_000300: -3.74e-1

QD
type: SiteQuality
SIO_000300: 2.342e1

GenotypeQuality
all individuals: 139
bin: 4.75e1
variant carriers: 17

GenotypeQuality
all individuals: 255
bin: 8.75e1
variant carriers: 26

GenotypeQuality
all individuals: 144
bin: 5.75e1
variant carriers: 23

GenotypeQuality
all individuals: 157
bin: 5.25e1
variant carriers: 24

GenotypeQuality
all individuals: 118
bin: 7.5e0
variant carriers: 26

GenotypeQuality
all individuals: 116
bin: 1.75e1
variant carriers: 23

GenotypeQuality
all individuals: 49483
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variant carriers: 4939

GenotypeQuality
all individuals: 1025
bin: 2.5e0
variant carriers: 19

GenotypeQuality
all individuals: 1306
bin: 6.75e1
variant carriers: 28

GenotypeQuality
all individuals: 417
bin: 8.25e1
variant carriers: 30

GenotypeQuality
all individuals: 136
bin: 4.25e1
variant carriers: 33

GenotypeQuality
all individuals: 147
bin: 2.75e1
variant carriers: 23

GenotypeQuality
all individuals: 113
bin: 1.25e1
variant carriers: 30

GenotypeQuality
all individuals: 238
bin: 2.25e1
variant carriers: 29

GenotypeQuality
all individuals: 141
bin: 3.25e1
variant carriers: 25

GenotypeQuality
all individuals: 542
bin: 7.75e1
variant carriers: 24

GenotypeQuality
all individuals: 355
bin: 9.25e1
variant carriers: 33

GenotypeQuality
all individuals: 157
bin: 3.75e1
variant carriers: 33

GenotypeQuality
all individuals: 5217
bin: 6.25e1
variant carriers: 26

European (Non-Finnish)
type: Population
allele count: 3083
allele frequency: 4.733464349321378e-2
allele num: 65132
num of homozygotes: 0

Latino
type: Population
allele count: 256
allele frequency: 2.24128874102609e-2
allele num: 11422
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 820
allele frequency: 1.265822784810127e-1
allele num: 6478
num of homozygotes: 0

East Asian
type: Population
allele count: 344
allele frequency: 4.02621722846442e-2
allele num: 8544
num of homozygotes: 0

South Asian
type: Population
allele count: 90
allele frequency: 5.459839844697889e-3
allele num: 16484
num of homozygotes: 0

African
type: Population
allele count: 687
allele frequency: 7.20125786163522e-2
allele num: 9540
num of homozygotes: 0

Other
type: Population
allele count: 68
allele frequency: 7.640449438202247e-2
allele num: 890
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.19e0

MQ
type: SiteQuality
SIO_000300: 5.942e1

FS
type: SiteQuality
SIO_000300: 1.43106e2

MQRankSum
type: SiteQuality
SIO_000300: -1.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.33e-2

DP
type: SiteQuality
SIO_000300: 6.17007e6

QD
type: SiteQuality
SIO_000300: 3.48e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.18e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.261e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.045e0

GenotypeQuality
all individuals: 50569
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 40
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 5862
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 516
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variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 38
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 631
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1495
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 541
bin: 8.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.41e0

MQRankSum
type: SiteQuality
SIO_000300: 4.83e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.938e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

MQ
type: SiteQuality
SIO_000300: 5.982e1

FS
type: SiteQuality
SIO_000300: 5.552e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.032e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e0

DP
type: SiteQuality
SIO_000300: 5.499906e6

QD
type: SiteQuality
SIO_000300: 9.449999999999999e0

GenotypeQuality
all individuals: 1495
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
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variant carriers: 0

GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 631
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variant carriers: 0

GenotypeQuality
all individuals: 50569
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 516
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variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 541
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5862
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 5.499906e6

FS
type: SiteQuality
SIO_000300: 5.552e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -6.032e0

MQ
type: SiteQuality
SIO_000300: 5.982e1

VQSLOD
type: SiteQuality
SIO_000300: -2.938e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e0

QD
type: SiteQuality
SIO_000300: 9.449999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.41e0

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 5843
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variant carriers: 0

GenotypeQuality
all individuals: 50566
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 516
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variant carriers: 0

GenotypeQuality
all individuals: 13
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GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 626
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variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
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variant carriers: 0

GenotypeQuality
all individuals: 43
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variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 540
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GenotypeQuality
all individuals: 448
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GenotypeQuality
all individuals: 1488
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 4
allele frequency: 4.622140050843541e-4
allele num: 8654
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.459609064175748e-4
allele num: 11562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66644
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 6.18e-1

FS
type: SiteQuality
SIO_000300: 1.522e0

QD
type: SiteQuality
SIO_000300: 1.403e1

VQSLOD
type: SiteQuality
SIO_000300: 6.889999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.46e-1

DP
type: SiteQuality
SIO_000300: 5.499255e6

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.21e0

GenotypeDepth
all individuals: 774
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
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variant carriers: 0

GenotypeQuality
all individuals: 228
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GenotypeQuality
all individuals: 1482
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variant carriers: 0

GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 54
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 5835
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GenotypeQuality
all individuals: 290
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GenotypeQuality
all individuals: 514
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GenotypeQuality
all individuals: 50565
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GenotypeQuality
all individuals: 537
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500600240096038e-5
allele num: 66640
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 7.84e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

MQRankSum
type: SiteQuality
SIO_000300: -7.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

DP
type: SiteQuality
SIO_000300: 5.497214e6

FS
type: SiteQuality
SIO_000300: 5.425e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.086e0

VQSLOD
type: SiteQuality
SIO_000300: 5.88e-1

QD
type: SiteQuality
SIO_000300: 1.424e1

GenotypeQuality
all individuals: 98
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variant carriers: 0

GenotypeQuality
all individuals: 20
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GenotypeQuality
all individuals: 5526
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GenotypeQuality
all individuals: 28
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GenotypeQuality
all individuals: 504
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GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 379
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GenotypeQuality
all individuals: 17
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GenotypeQuality
all individuals: 120
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GenotypeQuality
all individuals: 445
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GenotypeQuality
all individuals: 536
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variant carriers: 0

GenotypeQuality
all individuals: 50565
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 290
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variant carriers: 0

GenotypeQuality
all individuals: 616
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GenotypeQuality
all individuals: 1446
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501185936890143e-5
allele num: 66614
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.809e1

DP
type: SiteQuality
SIO_000300: 5.492968e6

VQSLOD
type: SiteQuality
SIO_000300: -2.073e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.9e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.87e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

FS
type: SiteQuality
SIO_000300: 1.222e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.630000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.0e-1

GenotypeQuality
all individuals: 578
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502494140272853e-5
allele num: 66556
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -1.46e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.693e0

MQ
type: SiteQuality
SIO_000300: 5.909e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

DP
type: SiteQuality
SIO_000300: 5.484141e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.0e0

FS
type: SiteQuality
SIO_000300: 1.1443e1

QD
type: SiteQuality
SIO_000300: 4.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e0

GenotypeQuality
all individuals: 82
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 2.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50271992306074e-5
allele num: 66546
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10156
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 7.2e0

VQSLOD
type: SiteQuality
SIO_000300: -6.879999999999999e-1

DP
type: SiteQuality
SIO_000300: 5.478863e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.3e-1

QD
type: SiteQuality
SIO_000300: 1.713e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.69e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

GenotypeQuality
all individuals: 195
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 595
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variant carriers: 0

GenotypeQuality
all individuals: 12
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 537

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 7.5e0
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GenotypeQuality
all individuals: 541
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 6
allele frequency: 5.920663114268798e-4
allele num: 10134
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 315
allele frequency: 3.641618497109827e-2
allele num: 8650
num of homozygotes: 5

Latino
type: Population
allele count: 158
allele frequency: 1.366545580349421e-2
allele num: 11562
num of homozygotes: 3

Other
type: Population
allele count: 1
allele frequency: 1.108647450110865e-3
allele num: 902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 39
allele frequency: 5.861488517494289e-4
allele num: 66536
num of homozygotes: 0

South Asian
type: Population
allele count: 26
allele frequency: 1.584399756246191e-3
allele num: 16410
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.471935e6

MQRankSum
type: SiteQuality
SIO_000300: 2.34e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.9e-2

QD
type: SiteQuality
SIO_000300: 1.744e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.45e-2

MQ
type: SiteQuality
SIO_000300: 5.984e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.6e0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1172
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GenotypeQuality
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GenotypeQuality
all individuals: 50553
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GenotypeQuality
all individuals: 252
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GenotypeQuality
all individuals: 316
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 31
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GenotypeQuality
all individuals: 285
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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: 3531
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variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10134
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66522
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.895e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

QD
type: SiteQuality
SIO_000300: 1.357e1

MQRankSum
type: SiteQuality
SIO_000300: 9.9e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.334e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.95e-1

DP
type: SiteQuality
SIO_000300: 5.444426e6

BaseQRankSum
type: SiteQuality
SIO_000300: -9.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.9e-1

GenotypeQuality
all individuals: 518
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 639
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 34
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503623733197005e-5
allele num: 66506
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16394
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

DP
type: SiteQuality
SIO_000300: 5.443234e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.8e0

MQ
type: SiteQuality
SIO_000300: 5.987e1

QD
type: SiteQuality
SIO_000300: 1.426e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.952e0

GenotypeQuality
all individuals: 587
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 499
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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: 29
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GenotypeQuality
all individuals: 516
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GenotypeQuality
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GenotypeQuality
all individuals: 280
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 486
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variant carriers: 0

GenotypeQuality
all individuals: 993
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504438092372499e-5
allele num: 66470
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16326
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9958
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.13e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.05e0

FS
type: SiteQuality
SIO_000300: 3.096e0

QD
type: SiteQuality
SIO_000300: 1.532e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.47e-1

DP
type: SiteQuality
SIO_000300: 5.434512e6

MQ
type: SiteQuality
SIO_000300: 5.941e1

VQSLOD
type: SiteQuality
SIO_000300: 8.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

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: 50552
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16272
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505253334136135e-5
allele num: 66434
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9954
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 3.175e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.37e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

DP
type: SiteQuality
SIO_000300: 5.434447e6

QD
type: SiteQuality
SIO_000300: 1.285e1

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

MQRankSum
type: SiteQuality
SIO_000300: 8.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.36e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 45
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GenotypeQuality
all individuals: 123
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variant carriers: 0

GenotypeQuality
all individuals: 535
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GenotypeQuality
all individuals: 531
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GenotypeQuality
all individuals: 443
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GenotypeQuality
all individuals: 844
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GenotypeQuality
all individuals: 567
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GenotypeQuality
all individuals: 373
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GenotypeQuality
all individuals: 346
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GenotypeQuality
all individuals: 1476
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GenotypeQuality
all individuals: 50550
bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9940
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505570611261668e-5
allele num: 66420
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16238
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.18e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.8e-2

MQ
type: SiteQuality
SIO_000300: 5.982e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.68e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.33e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.341e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

DP
type: SiteQuality
SIO_000300: 5.432867e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.72e-1

GenotypeQuality
all individuals: 123
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 844
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50550
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 373
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 860
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1476
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 531
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 959
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16238
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505570611261668e-5
allele num: 66420
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9940
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.33e0

QD
type: SiteQuality
SIO_000300: 1.341e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -5.72e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.18e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.8e-2

DP
type: SiteQuality
SIO_000300: 5.432867e6

GenotypeQuality
all individuals: 88
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 2.5e0
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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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GenotypeQuality
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bin: 3.75e1
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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: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 873
bin: 6.75e1
variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 14
allele frequency: 2.107291227647661e-4
allele num: 66436
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16260
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.051e0

QD
type: SiteQuality
SIO_000300: 1.412e1

MQ
type: SiteQuality
SIO_000300: 5.986e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.97e0

DP
type: SiteQuality
SIO_000300: 5.432586e6

GenotypeQuality
all individuals: 514
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1738
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16268
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9950
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -9.19e-1

FS
type: SiteQuality
SIO_000300: 3.51e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.7e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.975e1

DP
type: SiteQuality
SIO_000300: 5.43252e6

VQSLOD
type: SiteQuality
SIO_000300: -8.95e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.51e-1

QD
type: SiteQuality
SIO_000300: 1.444e1