16-7715002-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7715002
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7715002
    reference: chr 16
allele count: 1
allele frequency: 8.281847845891375e-6
allele num: 120746
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.951-6557G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.801+32G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.945+32G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.849+32G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1059+32G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.951-6557G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1059+32G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.930+32G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.930+32G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.981+32G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.951-6557G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.82+11053G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.205+32G>T
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2806
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff

16-7715004-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7715004
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7715004
    reference: chr 16
allele count: 1
allele frequency: 8.281710670156027e-6
allele num: 120748
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.205+34T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1059+34T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.951-6555T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.930+34T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.945+34T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1059+34T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.930+34T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.951-6555T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.849+34T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.801+34T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.951-6555T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.82+11055T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.981+34T>A
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42203
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2806
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

16-7715007-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7715007
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7715007
    reference: chr 16
allele count: 1
allele frequency: 8.281710670156027e-6
allele num: 120748
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.82+11058C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.205+37C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.945+37C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.951-6552C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.801+37C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.849+37C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1059+37C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.981+37C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.930+37C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.930+37C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.951-6552C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1059+37C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.951-6552C>T
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

16-7715012-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7715012
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7715012
    reference: chr 16
allele count: 1
allele frequency: 8.28239659427852e-6
allele num: 120738
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.930+42G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.981+42G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.801+42G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1059+42G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1059+42G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.945+42G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.951-6547G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.205+42G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.930+42G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.82+11063G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.951-6547G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.849+42G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.951-6547G>A
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2806
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42203
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

16-7715013-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7715013
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7715013
    reference: chr 16
allele count: 1
allele frequency: 8.28225940036442e-6
allele num: 120740
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.951-6546G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.981+43G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.945+43G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1059+43G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.849+43G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.82+11064G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.951-6546G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.801+43G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1059+43G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.951-6546G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.930+43G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.930+43G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.205+43G>C
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

16-7715013-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7715013
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7715013
    reference: chr 16
allele count: 1
allele frequency: 8.28225940036442e-6
allele num: 120740
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.951-6546G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.981+43G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.930+43G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1059+43G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.849+43G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.951-6546G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.951-6546G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.945+43G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.801+43G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.82+11064G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.205+43G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.930+43G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1059+43G>T
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42203
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

16-7715016-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7715016
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7715016
    reference: chr 16
allele count: 1
allele frequency: 8.282122210995345e-6
allele num: 120742
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.951-6543T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.981+46T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.951-6543T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.930+46T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.951-6543T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.801+46T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1059+46T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.82+11067T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.205+46T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.849+46T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.945+46T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.930+46T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1059+46T>A
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2806
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

16-7721510-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721510
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721510
    reference: chr 16
allele count: 1
allele frequency: 8.383775717232013e-6
allele num: 119278
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5266A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5266A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5266A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.951-49A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5266A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5266A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.951-49A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5266A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5266A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.951-49A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5266A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5266A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5266A>T
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8306
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3481
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12890
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4756
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13056
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-7721512-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721512
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721512
    reference: chr 16
allele count: 1
allele frequency: 8.370862701109976e-6
allele num: 119462
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5264T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5264T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.951-47T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5264T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5264T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5264T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5264T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5264T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5264T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.951-47T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.951-47T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5264T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5264T>A
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4764
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13717
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3463
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2955
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

16-7721514-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721514
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721514
    reference: chr 16
allele count: 1
allele frequency: 8.370302167908262e-6
allele num: 119470
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5262A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.951-45A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5262A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5262A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5262A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.951-45A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.951-45A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5262A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5262A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5262A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5262A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5262A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5262A>G
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4772
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14755
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8418
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13339
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

16-7721515-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721515
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721515
    reference: chr 16
allele count: 6
allele frequency: 5.019156447106456e-5
allele num: 119542
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5261T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.951-44T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5261T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5261T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5261T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5261T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.951-44T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.951-44T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5261T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5261T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5261T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5261T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5261T>G
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3365
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13402
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15341
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8422
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

16-7721518-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721518
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721518
    reference: chr 16
allele count: 1
allele frequency: 8.371563473194253e-6
allele num: 119452
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5258C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5258C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.951-41C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5258C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5258C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5258C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.951-41C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5258C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5258C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5258C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.951-41C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5258C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5258C>T
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16488
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2960
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13675
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8531
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP

16-7721519-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721519
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721519
    reference: chr 16
allele count: 2
allele frequency: 1.673276107290464e-5
allele num: 119526
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5257A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5257A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5257A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.951-40A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5257A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5257A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5257A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5257A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.951-40A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5257A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5257A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.951-40A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5257A>T
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2946
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8544
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2633
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2961
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13828
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16956
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

16-7721528-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721528
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721528
    reference: chr 16
allele count: 1
allele frequency: 8.347245409015026e-6
allele num: 119800
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.951-31T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5248T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5248T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5248T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5248T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5248T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5248T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5248T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5248T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5248T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.951-31T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5248T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.951-31T>C
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2965
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19555
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14472
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

16-7721531-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721531
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721531
    reference: chr 16
allele count: 1
allele frequency: 8.340700952508049e-6
allele num: 119894
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5245A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5245A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5245A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5245A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.951-28A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5245A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5245A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.951-28A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5245A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5245A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.951-28A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5245A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5245A>T
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4812
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14683
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8736
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19918
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2967
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS

16-7721534-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721534
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721534
    reference: chr 16
allele count: 3
allele frequency: 2.499875006249687e-5
allele num: 120006
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5242A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5242A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5242A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5242A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.951-25A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5242A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5242A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5242A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5242A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5242A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5242A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.951-25A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.951-25A>G
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20218
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14779
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2970
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ

16-7721535-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721535
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721535
    reference: chr 16
allele count: 2
allele frequency: 1.666055779547499e-5
allele num: 120044
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5241C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.951-24C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5241C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.951-24C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5241C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5241C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5241C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.951-24C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5241C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5241C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5241C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5241C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5241C>T
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14822
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8746
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4819
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff

16-7721536-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721536
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721536
    reference: chr 16
allele count: 1
allele frequency: 8.326671995736744e-6
allele num: 120096
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5240A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5240A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5240A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5240A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5240A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5240A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5240A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5240A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5240A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5240A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.951-23A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.951-23A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.951-23A>G
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8746
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2972
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20383
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14871
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP

16-7721538-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721538
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721538
    reference: chr 16
allele count: 1
allele frequency: 8.320575118152166e-6
allele num: 120184
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5238T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5238T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.951-21T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5238T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5238T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5238T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5238T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.951-21T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.951-21T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5238T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5238T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5238T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5238T>G
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4821
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20515
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8764
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2969
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

16-7721547-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721547
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721547
    reference: chr 16
allele count: 1
allele frequency: 8.300959590928711e-6
allele num: 120468
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5229G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5229G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5229G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5229G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.951-12G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5229G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.951-12G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5229G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.951-12G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5229G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5229G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5229G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5229G>A
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15148
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20848
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD

16-7721547-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721547
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721547
    reference: chr 16
allele count: 4
allele frequency: 3.320383836371484e-5
allele num: 120468
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5229G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5229G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5229G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.951-12G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5229G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.951-12G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5229G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5229G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.951-12G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5229G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5229G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5229G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5229G>C
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15148
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20848
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4829
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD

16-7721550-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721550
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721550
    reference: chr 16
allele count: 1
allele frequency: 8.295450774795103e-6
allele num: 120548
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5226T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5226T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5226T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5226T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5226T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.951-9T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5226T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5226T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5226T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5226T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.951-9T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5226T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.951-9T>C
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4825
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8790
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15187
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2969
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20934
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

16-7721552-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721552
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721552
    reference: chr 16
allele count: 10
allele frequency: 8.292424041395781e-5
allele num: 120592
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5224C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5224C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5224C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5224C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5224C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5224C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5224C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.951-7C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.951-7C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5224C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5224C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.951-7C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5224C>T
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2969
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4831
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8797
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 15227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20948
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: c.951-7C>T
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP

16-7721558-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721558
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721558
    reference: chr 16
allele count: 1
allele frequency: 8.285278716776033e-6
allele num: 120696
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.951-1G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.951-1G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5218G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5218G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5218G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.951-1G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5218G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5218G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5218G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5218G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5218G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5218G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5218G>C
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8806
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15287
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2970
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4832
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.951-1G>C
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

16-7721567-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721567
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721567
    reference: chr 16
allele count: 1
allele frequency: 8.274994621253496e-6
allele num: 120846
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.959A>G
  hgvsp: ENSP00000309117.5:p.Tyr320Cys
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.959A>G
  hgvsp: ENSP00000402745.2:p.Tyr320Cys
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5209A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5209A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5209A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5209A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5209A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.959A>G
  hgvsp: ENSP00000347855.4:p.Tyr320Cys
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5209A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5209A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5209A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5209A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5209A>G
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2968
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4828
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8815
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr320Cys
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQ

16-7721568-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721568
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721568
    reference: chr 16
allele count: 1
allele frequency: 8.27417299640901e-6
allele num: 120858
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5208T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5208T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5208T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5208T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5208T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5208T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.960T>A
  hgvsp: ENSP00000347855.4:p.Tyr320Ter
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.960T>A
  hgvsp: ENSP00000402745.2:p.Tyr320Ter
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.960T>A
  hgvsp: ENSP00000309117.5:p.Tyr320Ter
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5208T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5208T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5208T>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5208T>A
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2968
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4827
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8815
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15410
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr320Ter
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff

16-7721570-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721570
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721570
    reference: chr 16
allele count: 1
allele frequency: 8.272667107875579e-6
allele num: 120880
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5206A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.962A>G
  hgvsp: ENSP00000402745.2:p.Gln321Arg
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.962A>G
  hgvsp: ENSP00000347855.4:p.Gln321Arg
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5206A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.962A>G
  hgvsp: ENSP00000309117.5:p.Gln321Arg
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5206A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5206A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5206A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5206A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5206A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5206A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5206A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5206A>G
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4829
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21003
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8815
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2968
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln321Arg
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

16-7721585-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721585
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721585
    reference: chr 16
allele count: 1
allele frequency: 8.269246671628215e-6
allele num: 120930
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.977G>T
  hgvsp: ENSP00000402745.2:p.Gly326Val
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5191G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.977G>T
  hgvsp: ENSP00000347855.4:p.Gly326Val
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5191G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.977G>T
  hgvsp: ENSP00000309117.5:p.Gly326Val
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5191G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5191G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5191G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5191G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5191G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5191G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5191G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5191G>T
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8844
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4838
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20768
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15568
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly326Val
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ

16-7721601-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721601
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721601
    reference: chr 16
allele count: 1
allele frequency: 8.272119647938589e-6
allele num: 120888
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5175G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5175G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5175G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.993G>A
  hgvsp: ENST00000436368.2:c.993G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5175G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.993G>A
  hgvsp: ENST00000311745.5:c.993G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5175G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.993G>A
  hgvsp: ENST00000355637.4:c.993G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5175G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5175G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5175G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5175G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5175G>A
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15633
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20383
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2968
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4836
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8823
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.993G>A
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

16-7721602-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721602
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721602
    reference: chr 16
allele count: 1
allele frequency: 8.272940865018697e-6
allele num: 120876
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.993+1G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5174G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5174G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5174G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5174G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5174G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5174G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5174G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.993+1G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.993+1G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5174G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5174G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5174G>C
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15632
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20331
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2969
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.993+1G>C
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum

16-7721606-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721606
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721606
    reference: chr 16
allele count: 1
allele frequency: 8.274583788435442e-6
allele num: 120852
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5170G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.993+5G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5170G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5170G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.993+5G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5170G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5170G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5170G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.993+5G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5170G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5170G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5170G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5170G>T
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2969
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8827
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20102
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4836
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.993+5G>T
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

16-7721609-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721609
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721609
    reference: chr 16
allele count: 1
allele frequency: 8.276364358664525e-6
allele num: 120826
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5167A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5167A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5167A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5167A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5167A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5167A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.993+8A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5167A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.993+8A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.993+8A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5167A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5167A>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5167A>T
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15604
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8815
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19929
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4832
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2968
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.993+8A>T
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

16-7721613-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721613
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721613
    reference: chr 16
allele count: 11
allele frequency: 9.109127345600292e-5
allele num: 120758
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5163C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.993+12C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5163C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5163C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5163C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5163C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5163C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5163C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.993+12C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5163C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5163C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.993+12C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5163C>T
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2970
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15593
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19457
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4846
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8843
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

16-7721614-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721614
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721614
    reference: chr 16
allele count: 5
allele frequency: 4.141335497871354e-5
allele num: 120734
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5162G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5162G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5162G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5162G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5162G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.993+13G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5162G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5162G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5162G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5162G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.993+13G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5162G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.993+13G>A
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4849
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8848
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2968
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum

16-7721615-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721615
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721615
    reference: chr 16
allele count: 17
allele frequency: 1.407704282733265e-4
allele num: 120764
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5161A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.993+14A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.993+14A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.993+14A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5161A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5161A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5161A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5161A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5161A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5161A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5161A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5161A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5161A>G
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15590
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19164
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/16-7721616-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721616
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721616
    reference: chr 16
allele count: 1
allele frequency: 8.281710670156027e-6
allele num: 120748
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5160C>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5160C>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.993+15C>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5160C>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5160C>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5160C>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5160C>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.993+15C>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5160C>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5160C>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5160C>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5160C>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.993+15C>A
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19153
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2965
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8832
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

16-7721617-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721617
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721617
    reference: chr 16
allele count: 3
allele frequency: 2.484595507851322e-5
allele num: 120744
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5159T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5159T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.993+16T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.993+16T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5159T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.993+16T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5159T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5159T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5159T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5159T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5159T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5159T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5159T>C
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8820
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4843
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2964
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15555
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

16-7721618-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721618
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721618
    reference: chr 16
allele count: 1
allele frequency: 8.282808203293245e-6
allele num: 120732
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5158G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5158G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.993+17G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5158G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5158G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5158G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5158G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5158G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5158G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5158G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5158G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.993+17G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.993+17G>A
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4851
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18896
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15538
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8837
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

16-7721619-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721619
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721619
    reference: chr 16
allele count: 6
allele frequency: 4.969767249233827e-5
allele num: 120730
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5157G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.993+18G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5157G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5157G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5157G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5157G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5157G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.993+18G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5157G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5157G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5157G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.993+18G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5157G>C
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4848
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18799
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15519
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff

16-7721619-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721619
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721619
    reference: chr 16
allele count: 1
allele frequency: 8.282945415389712e-6
allele num: 120730
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5157G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5157G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.993+18G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5157G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5157G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5157G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5157G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.993+18G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5157G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5157G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.993+18G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5157G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5157G>T
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4848
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18799
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15519
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2968
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ

16-7721628-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721628
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721628
    reference: chr 16
allele count: 1
allele frequency: 8.289262089888757e-6
allele num: 120638
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.993+27C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5148C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5148C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5148C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5148C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5148C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5148C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5148C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5148C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5148C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.993+27C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.993+27C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5148C>G
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15178
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8812
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4842
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2968
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

16-7721629-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721629
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721629
    reference: chr 16
allele count: 2
allele frequency: 1.658182300562124e-5
allele num: 120614
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5147T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5147T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5147T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5147T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5147T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.993+28T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5147T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.993+28T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5147T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5147T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5147T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.993+28T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5147T>G
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4840
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8799
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17319
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15156
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2968
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

16-7721635-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721635
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721635
    reference: chr 16
allele count: 9
allele frequency: 7.464171974522293e-5
allele num: 120576
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5141C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5141C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.993+34C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.993+34C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5141C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5141C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5141C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5141C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.993+34C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5141C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5141C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5141C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5141C>G
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8796
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16214
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4842
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2967
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14849
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

16-7721635-CTA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721635
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721633
    reference: chr 16
allele count: 1
allele frequency: 8.293524416135881e-6
allele num: 120576
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5139_982-5138delAT
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.993+36_993+37delAT
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5139_1060-5138delAT
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5139_931-5138delAT
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5139_206-5138delAT
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5139_1060-5138delAT
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5139_850-5138delAT
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5139_802-5138delAT
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5139_931-5138delAT
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.993+36_993+37delAT
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5139_83-5138delAT
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5139_946-5138delAT
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.993+36_993+37delAT
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16214
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4842
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8796
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2967
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
reference allele: CTA
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

16-7721637-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721637
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721637
    reference: chr 16
allele count: 3
allele frequency: 2.488222413907504e-5
allele num: 120568
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5139A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.993+36A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5139A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5139A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5139A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5139A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.993+36A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5139A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5139A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5139A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5139A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5139A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.993+36A>G
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4839
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8746
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14723
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum

16-7721641-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721641
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721641
    reference: chr 16
allele count: 1
allele frequency: 8.29737802854298e-6
allele num: 120520
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5135T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5135T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.993+40T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5135T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5135T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5135T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.993+40T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5135T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.993+40T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5135T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5135T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5135T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5135T>C
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4838
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8707
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14821
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14164
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5621
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2965
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2025
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

16-7721641-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721641
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721641
    reference: chr 16
allele count: 1
allele frequency: 8.29737802854298e-6
allele num: 120520
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5135T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.993+40T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5135T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5135T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5135T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5135T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5135T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5135T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5135T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.993+40T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5135T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5135T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.993+40T>G
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14164
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14821
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8707
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2025
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4838
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2965
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

16-7721647-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721647
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721647
    reference: chr 16
allele count: 3
allele frequency: 2.493019545273235e-5
allele num: 120336
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5129G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5129G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5129G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5129G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5129G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5129G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5129G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5129G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.993+46G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.993+46G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5129G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5129G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.993+46G>T
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13463
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5711
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15494
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4843
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8597
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

16-7721649-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721649
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721649
    reference: chr 16
allele count: 1
allele frequency: 8.30592378484335e-6
allele num: 120396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5127T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5127T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5127T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5127T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5127T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5127T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5127T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5127T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.993+48T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5127T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.993+48T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.993+48T>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5127T>G
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4842
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8521
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2045
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

16-7721651-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7721651
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7721651
    reference: chr 16
allele count: 1
allele frequency: 8.31766839119658e-6
allele num: 120226
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-5125G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-5125G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-5125G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.993+50G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-5125G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-5125G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-5125G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-5125G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-5125G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.993+50G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-5125G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.993+50G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-5125G>C
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13403
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4840
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15649
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5672
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8525
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

16-7726725-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7726725
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7726725
    reference: chr 16
allele count: 5154
allele frequency: 4.266626930909452e-2
allele num: 120798
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.994-51C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-51C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-51C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-51C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-51C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-51C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.994-51C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-51C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-51C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-51C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.994-51C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-51C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-51C>G
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4310
  bin: 2.25e1
  variant carriers: 307
genotype depth: GenotypeDepth
  all individuals: 11101
  bin: 2.75e1
  variant carriers: 593
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 4.75e1
  variant carriers: 462
genotype depth: GenotypeDepth
  all individuals: 9782
  bin: 3.75e1
  variant carriers: 829
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 1.75e1
  variant carriers: 136
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.25e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 6.75e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 8.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 9.75e1
  variant carriers: 213
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12970
  bin: 3.25e1
  variant carriers: 792
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 5.25e1
  variant carriers: 314
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 6527
  bin: 4.25e1
  variant carriers: 616
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 6.25e1
  variant carriers: 127
genotype quality: GenotypeQuality
num of homozygotes: 272
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

16-7726725-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7726725
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7726725
    reference: chr 16
allele count: 1
allele frequency: 8.278282753025713e-6
allele num: 120798
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-51C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.994-51C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.994-51C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-51C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-51C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-51C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-51C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-51C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-51C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-51C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-51C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.994-51C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-51C>T
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11101
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12970
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9782
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4310
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

16-7726734-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7726734
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7726734
    reference: chr 16
allele count: 56
allele frequency: 4.628405183813806e-4
allele num: 120992
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.994-42G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-42G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-42G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-42G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-42G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.994-42G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-42G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-42G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-42G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-42G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.994-42G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-42G>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-42G>T
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2213
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6402
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 13409
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9796
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4910
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11610
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP

16-7726738-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7726738
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7726738
    reference: chr 16
allele count: 5
allele frequency: 4.131889926452359e-5
allele num: 121010
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-38C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-38C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-38C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-38C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-38C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-38C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-38C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-38C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.994-38C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-38C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.994-38C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-38C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.994-38C>T
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9811
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11772
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13541
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6402
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS

16-7726739-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7726739
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7726739
    reference: chr 16
allele count: 2
allele frequency: 1.652537471287161e-5
allele num: 121026
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-37G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-37G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.994-37G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-37G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-37G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.994-37G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-37G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-37G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-37G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-37G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-37G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.994-37G>A
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-37G>A
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9821
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3784
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13577
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

16-7726743-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7726743
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7726743
    reference: chr 16
allele count: 1
allele frequency: 8.258729477057249e-6
allele num: 121084
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-33C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.994-33C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-33C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.994-33C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-33C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-33C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-33C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-33C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-33C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-33C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.994-33C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-33C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-33C>T
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9830
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13646
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11902
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5156
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6409
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

16-7726747-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7726747
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7726747
    reference: chr 16
allele count: 2
allele frequency: 1.651336757104876e-5
allele num: 121114
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-29C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-29C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-29C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.994-29C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-29C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-29C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.994-29C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.994-29C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-29C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-29C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-29C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-29C>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-29C>G
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9837
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13678
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11919
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6408
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5217
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3792
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

16-7726747-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7726747
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7726747
    reference: chr 16
allele count: 5
allele frequency: 4.128341892762191e-5
allele num: 121114
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.994-29C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-29C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-29C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-29C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-29C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-29C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-29C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.994-29C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-29C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-29C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.994-29C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-29C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-29C>T
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11919
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6408
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13678
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9837
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5217
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

16-7726749-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7726749
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7726749
    reference: chr 16
allele count: 3
allele frequency: 2.476309967973058e-5
allele num: 121148
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.994-27T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-27T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-27T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-27T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.994-27T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-27T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-27T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-27T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-27T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-27T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.994-27T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-27T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-27T>C
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6413
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11938
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3794
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9834
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

16-7726756-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7726756
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7726756
    reference: chr 16
allele count: 1
allele frequency: 8.250688932525866e-6
allele num: 121202
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.994-20C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-20C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-20C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.994-20C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-20C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-20C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-20C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.994-20C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-20C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-20C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-20C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-20C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-20C>T
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5241
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11987
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9837
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6413
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

16-7726757-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7726757
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7726757
    reference: chr 16
allele count: 15484
allele frequency: 1.277262678589105e-1
allele num: 121228
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-19A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-19A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-19A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-19A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-19A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-19A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.994-19A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-19A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.994-19A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-19A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.994-19A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-19A>G
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-19A>G
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 6.25e1
  variant carriers: 1543
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 3775
  bin: 4.75e1
  variant carriers: 1075
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 7.75e1
  variant carriers: 961
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 2.25e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 8.25e1
  variant carriers: 720
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9776
  bin: 2.75e1
  variant carriers: 130
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 6.75e1
  variant carriers: 1296
genotype depth: GenotypeDepth
  all individuals: 7881
  bin: 3.75e1
  variant carriers: 468
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 8.75e1
  variant carriers: 513
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 9.25e1
  variant carriers: 356
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 7.25e1
  variant carriers: 1170
genotype depth: GenotypeDepth
  all individuals: 2993
  bin: 5.25e1
  variant carriers: 1397
genotype depth: GenotypeDepth
  all individuals: 11098
  bin: 3.25e1
  variant carriers: 239
genotype quality: GenotypeQuality
num of homozygotes: 1076
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

16-7726761-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7726761
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7726761
    reference: chr 16
allele count: 1
allele frequency: 8.246742536698004e-6
allele num: 121260
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-15C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.994-15C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-15C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-15C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-15C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-15C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-15C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-15C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-15C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-15C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.994-15C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-15C>T
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.994-15C>T
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9896
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14340
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3692
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-7726767-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7726767
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7726767
    reference: chr 16
allele count: 3
allele frequency: 2.473696362017217e-5
allele num: 121276
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-9G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.994-9G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.994-9G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-9G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-9G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-9G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-9G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-9G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-9G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.994-9G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-9G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-9G>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-9G>C
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14343
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3691
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9896
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

16-7726768-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7726768
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7726768
    reference: chr 16
allele count: 1
allele frequency: 8.245246615326264e-6
allele num: 121282
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.802-8T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.931-8T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.994-8T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.83-8T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.982-8T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.946-8T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1060-8T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.994-8T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.206-8T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1060-8T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.850-8T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.994-8T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.931-8T>C
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12566
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14342
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4125
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.994-8T>C
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD

16-7726778-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7726778
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7726778
    reference: chr 16
allele count: 1
allele frequency: 8.243615319934711e-6
allele num: 121306
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1062T>C
  hgvsp: ENST00000547372.1:c.1062T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.933T>C
  hgvsp: ENST00000550418.1:c.933T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.948T>C
  hgvsp: ENST00000340209.4:c.948T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.984T>C
  hgvsp: ENST00000552089.1:c.984T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.996T>C
  hgvsp: ENST00000311745.5:c.996T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.996T>C
  hgvsp: ENST00000436368.2:c.996T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.208T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.85T>C
  hgvsp: ENSP00000454250.1:p.Val29Ala
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.852T>C
  hgvsp: ENST00000553186.1:c.852T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1062T>C
  hgvsp: ENST00000422070.4:c.1062T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.996T>C
  hgvsp: ENST00000355637.4:c.996T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.804T>C
  hgvsp: ENST00000535565.2:c.804T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.933T>C
  hgvsp: ENST00000547338.1:c.933T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18222
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3691
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4142
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6180
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14350
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val29Ala
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum

16-7726782-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7726782
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 7726782
    reference: chr 16
allele count: 1
allele frequency: 8.24347940778844e-6
allele num: 121308
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000450031
  ensembl transcript: ENST00000550418
  gene symbol: RBFOX1
  hgvsc: ENST00000550418.1:c.937T>C
  hgvsp: ENSP00000450031.1:p.Tyr313His
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000309117
  ensembl transcript: ENST00000311745
  gene symbol: RBFOX1
  hgvsc: ENST00000311745.5:c.1000T>C
  hgvsp: ENSP00000309117.5:p.Tyr334His
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000454250
  ensembl transcript: ENST00000567470
  gene symbol: RBFOX1
  hgvsc: ENST00000567470.1:c.89T>C
  hgvsp: ENST00000567470.1:c.89T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000344196
  ensembl transcript: ENST00000340209
  gene symbol: RBFOX1
  hgvsc: ENST00000340209.4:c.952T>C
  hgvsp: ENSP00000344196.4:p.Tyr318His
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000448496
  ensembl transcript: ENST00000552089
  gene symbol: RBFOX1
  hgvsc: ENST00000552089.1:c.988T>C
  hgvsp: ENSP00000448496.1:p.Tyr330His
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000446842
  ensembl transcript: ENST00000547372
  gene symbol: RBFOX1
  hgvsc: ENST00000547372.1:c.1066T>C
  hgvsp: ENSP00000446842.1:p.Tyr356His
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078328
  ensembl transcript: ENST00000570188
  gene symbol: RBFOX1
  hgvsc: ENST00000570188.1:n.212T>C
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447717
  ensembl transcript: ENST00000547338
  gene symbol: RBFOX1
  hgvsc: ENST00000547338.1:c.937T>C
  hgvsp: ENSP00000447717.1:p.Tyr313His
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000347855
  ensembl transcript: ENST00000355637
  gene symbol: RBFOX1
  hgvsc: ENST00000355637.4:c.1000T>C
  hgvsp: ENSP00000347855.4:p.Tyr334His
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000438768
  ensembl transcript: ENST00000535565
  gene symbol: RBFOX1
  hgvsc: ENST00000535565.2:c.808T>C
  hgvsp: ENSP00000438768.2:p.Tyr270His
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000391269
  ensembl transcript: ENST00000422070
  gene symbol: RBFOX1
  hgvsc: ENST00000422070.4:c.1066T>C
  hgvsp: ENSP00000391269.4:p.Tyr356His
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000402745
  ensembl transcript: ENST00000436368
  gene symbol: RBFOX1
  hgvsc: ENST00000436368.2:c.1000T>C
  hgvsp: ENSP00000402745.2:p.Tyr334His
  variant of: http://identifiers.org/hgnc/18222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078328
  ensembl protein: ENSP00000447753
  ensembl transcript: ENST00000553186
  gene symbol: RBFOX1
  hgvsc: ENST00000553186.1:c.856T>C
  hgvsp: ENSP00000447753.1:p.Tyr286His
  variant of: http://identifiers.org/hgnc/18222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14355
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6180
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3691
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4131
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr334His
num of homozygotes: 0
population: Latino
reference allele: T

GenotypeDepth
all individuals: 1094
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 42203
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1138
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58730
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 236
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 145
bin: 7.25e1
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: 0
allele frequency: 0.0e0
allele num: 11564
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: 898
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.04e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.056e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.967e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.619e0

QD
type: SiteQuality
SIO_000300: 1.406e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.08e-1

FS
type: SiteQuality
SIO_000300: 2.301e0

DP
type: SiteQuality
SIO_000300: 7.148497e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

GenotypeDepth
all individuals: 1285
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1138
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1090
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 236
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58730
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
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: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.01e-1

DP
type: SiteQuality
SIO_000300: 7.148395e6

MQRankSum
type: SiteQuality
SIO_000300: -1.04e0

FS
type: SiteQuality
SIO_000300: 1.259e0

QD
type: SiteQuality
SIO_000300: 1.187e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.792e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

GenotypeDepth
all individuals: 42203
bin: 9.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 1091
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58730
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 39
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 7.148221e6

QD
type: SiteQuality
SIO_000300: 1.437e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.53e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.149e0

VQSLOD
type: SiteQuality
SIO_000300: -8.317e-1

FS
type: SiteQuality
SIO_000300: 1.0522e1

MQ
type: SiteQuality
SIO_000300: 5.974e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.929e0

GenotypeDepth
all individuals: 1043
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1094
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2448
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 236
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 191
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 142
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58730
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 263
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 177
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
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: 11556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.505e0

MQRankSum
type: SiteQuality
SIO_000300: 3.75e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

DP
type: SiteQuality
SIO_000300: 7.148033e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.3e-1

FS
type: SiteQuality
SIO_000300: 9.755000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -4.056e-1

QD
type: SiteQuality
SIO_000300: 1.422e1

GenotypeDepth
all individuals: 2807
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 42203
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1091
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 166
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 58730
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.655011251514626e-5
allele num: 11554
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: 9800
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.243e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.52e-1

QD
type: SiteQuality
SIO_000300: 1.318e1

MQRankSum
type: SiteQuality
SIO_000300: 7.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.27e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e0

DP
type: SiteQuality
SIO_000300: 7.148036e6

MQ
type: SiteQuality
SIO_000300: 5.968e1

GenotypeDepth
all individuals: 1091
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2807
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1094
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 237
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 58730
bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Latino
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European (Non-Finnish)
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allele num: 66738
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Other
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ClippingRankSum
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BaseQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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MQ
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QD
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MQRankSum
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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African
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European (Finnish)
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Latino
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East Asian
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Other
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InbreedingCoeff
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VQSLOD
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FS
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MQ
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ReadPosRankSum
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QD
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DP
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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European (Non-Finnish)
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South Asian
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African
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East Asian
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Latino
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MQ
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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FS
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DP
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VQSLOD
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QD
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65596
num of homozygotes: 0

Other
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African
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European (Finnish)
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East Asian
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South Asian
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Latino
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ClippingRankSum
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ReadPosRankSum
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QD
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MQRankSum
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FS
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MQ
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16322
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10220
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.047851264858275e-5
allele num: 65620
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.085e0

DP
type: SiteQuality
SIO_000300: 1.963565e6

BaseQRankSum
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SIO_000300: -6.860000000000001e-1

FS
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MQRankSum
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SIO_000300: -5.12e-1

InbreedingCoeff
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SIO_000300: 7.0e-4

ClippingRankSum
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SIO_000300: -1.674e0

VQSLOD
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SIO_000300: 2.55e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

QD
type: SiteQuality
SIO_000300: 1.533e1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 16352
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11422
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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.75609756097561e-5
allele num: 10250
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.965e1

FS
type: SiteQuality
SIO_000300: 2.347e0

BaseQRankSum
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DP
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SIO_000300: 1.993216e6

VQSLOD
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SIO_000300: 1.1e0

MQRankSum
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SIO_000300: -6.3e-2

ReadPosRankSum
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SIO_000300: 1.53e-1

InbreedingCoeff
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SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.1e-2

QD
type: SiteQuality
SIO_000300: 1.08e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65842
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

South Asian
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allele frequency: 6.113216774666829e-5
allele num: 16358
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

MQRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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ClippingRankSum
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SIO_000300: 1.45e-1

QD
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DP
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SIO_000300: 2.00014e6

BaseQRankSum
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SIO_000300: -4.116e0

FS
type: SiteQuality
SIO_000300: 9.129e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16378
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.921129503407984e-4
allele num: 10270
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65912
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8538
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.71e-1

BaseQRankSum
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ReadPosRankSum
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VQSLOD
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QD
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ClippingRankSum
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SIO_000300: 2.71e-1

InbreedingCoeff
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SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
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SIO_000300: 2.004279e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 896
num of homozygotes: 0

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

African
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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: 2
allele frequency: 3.033060357901122e-5
allele num: 65940
num of homozygotes: 0

Latino
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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South Asian
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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MQ
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QD
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MQRankSum
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BaseQRankSum
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FS
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SIO_000300: 0.0e0

DP
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InbreedingCoeff
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SIO_000300: -2.0e-4

GenotypeDepth
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variant carriers: 0

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

African
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allele frequency: 9.733307377846993e-5
allele num: 10274
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

African
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East Asian
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66030
num of homozygotes: 0

South Asian
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European (Finnish)
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allele frequency: 0.0e0
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DP
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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FS
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BaseQRankSum
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MQ
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MQRankSum
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QD
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.510300247689241e-5
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African
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Latino
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VQSLOD
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BaseQRankSum
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FS
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQ
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DP
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66212
num of homozygotes: 0

Latino
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East Asian
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South Asian
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allele frequency: 2.436647173489279e-4
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European (Finnish)
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allele frequency: 0.0e0
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African
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Other
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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FS
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DP
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ReadPosRankSum
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ClippingRankSum
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MQ
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MQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

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

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10
allele frequency: 6.087909411907951e-4
allele num: 16426
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

Other
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Latino
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allele frequency: 0.0e0
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African
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: -8.03e-1

ReadPosRankSum
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FS
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SIO_000300: 1.963e0

VQSLOD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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QD
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

African
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European (Non-Finnish)
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Latino
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East Asian
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South Asian
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DP
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VQSLOD
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MQ
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ReadPosRankSum
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FS
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MQRankSum
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BaseQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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African
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European (Finnish)
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European (Non-Finnish)
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Latino
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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DP
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
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QD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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Other
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European (Finnish)
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South Asian
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African
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VQSLOD
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QD
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InbreedingCoeff
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ReadPosRankSum
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MQ
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MQRankSum
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FS
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ClippingRankSum
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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East Asian
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European (Non-Finnish)
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Other
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European (Finnish)
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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MQRankSum
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FS
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DP
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MQ
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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European (Finnish)
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East Asian
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Latino
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African
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South Asian
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InbreedingCoeff
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DP
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MQRankSum
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ReadPosRankSum
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QD
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ClippingRankSum
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FS
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VQSLOD
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MQ
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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Latino
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South Asian
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African
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European (Non-Finnish)
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InbreedingCoeff
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MQRankSum
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QD
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BaseQRankSum
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DP
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VQSLOD
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MQ
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ReadPosRankSum
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FS
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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African
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European (Non-Finnish)
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Latino
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South Asian
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VQSLOD
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QD
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BaseQRankSum
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MQRankSum
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FS
type: SiteQuality
SIO_000300: 7.016e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.2e-2

InbreedingCoeff
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SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.017375e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.36e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66362
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

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

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

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
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SIO_000300: 9.26e0

DP
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ClippingRankSum
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SIO_000300: -1.91e-1

ReadPosRankSum
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FS
type: SiteQuality
SIO_000300: 5.659999999999999e-1

BaseQRankSum
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SIO_000300: -1.035e0

MQ
type: SiteQuality
SIO_000300: 5.924e1

VQSLOD
type: SiteQuality
SIO_000300: 2.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.2e-1

GenotypeDepth
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variant carriers: 1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66372
num of homozygotes: 0

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

South Asian
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allele frequency: 9.738283627510651e-4
allele num: 16430
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 8.706251088281386e-5
allele num: 11486
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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MQRankSum
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QD
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VQSLOD
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SIO_000300: 1.86e0

ClippingRankSum
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SIO_000300: -2.3e-2

FS
type: SiteQuality
SIO_000300: 1.2e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.99e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e-1

DP
type: SiteQuality
SIO_000300: 2.013769e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6999
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66368
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.090875867949811e-5
allele num: 16418
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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 4.27e-1

DP
type: SiteQuality
SIO_000300: 2.013714e6

MQRankSum
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SIO_000300: -9.25e-1

QD
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BaseQRankSum
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VQSLOD
type: SiteQuality
SIO_000300: 3.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

FS
type: SiteQuality
SIO_000300: 4.936e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

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

Latino
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allele count: 2
allele frequency: 1.741553465691397e-4
allele num: 11484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506977304921788e-5
allele num: 66358
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQ
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DP
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FS
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ReadPosRankSum
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BaseQRankSum
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QD
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MQRankSum
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VQSLOD
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ClippingRankSum
type: SiteQuality
SIO_000300: -8.64e-1

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 1
allele frequency: 9.63020030816641e-5
allele num: 10384
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

European (Finnish)
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InbreedingCoeff
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MQ
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VQSLOD
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ReadPosRankSum
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FS
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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DP
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6
allele frequency: 5.779233288383741e-4
allele num: 10382
num of homozygotes: 0

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

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

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

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

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.709284096847239e-5
allele num: 11482
num of homozygotes: 0

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

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

MQRankSum
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SIO_000300: 3.0e-1

ReadPosRankSum
type: SiteQuality
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QD
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SIO_000300: 1.178e1

ClippingRankSum
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SIO_000300: -2.7e-1

InbreedingCoeff
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SIO_000300: 5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 2.566e0

VQSLOD
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SIO_000300: 2.62e0

DP
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SIO_000300: 2.010636e6

BaseQRankSum
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SIO_000300: 1.33e0

MQ
type: SiteQuality
SIO_000300: 5.982e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7.5e0
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GenotypeQuality
all individuals: 11506
bin: 9.75e1
variant carriers: 1

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

African
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allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.508477644361311e-5
allele num: 66292
num of homozygotes: 0

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

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

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

ClippingRankSum
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QD
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InbreedingCoeff
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BaseQRankSum
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FS
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SIO_000300: 3.877e0

MQRankSum
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SIO_000300: 8.41e-1

MQ
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SIO_000300: 5.906e1

ReadPosRankSum
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SIO_000300: 2.8e-1

VQSLOD
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SIO_000300: -1.901e0

DP
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SIO_000300: 1.998553e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 16396
num of homozygotes: 0

African
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allele count: 2
allele frequency: 1.926411096127914e-4
allele num: 10382
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66280
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.98e-1

VQSLOD
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DP
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SIO_000300: 1.996821e6

MQ
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SIO_000300: 5.974e1

FS
type: SiteQuality
SIO_000300: 5.8e-1

ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: 1.09e-2

BaseQRankSum
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SIO_000300: 4.33e-1

QD
type: SiteQuality
SIO_000300: 1.367e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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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: 9

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16396
num of homozygotes: 0

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

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

Latino
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allele count: 8
allele frequency: 6.978367062107466e-4
allele num: 11464
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.509160604871571e-5
allele num: 66262
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.48e-1

FS
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SIO_000300: 1.321e0

DP
type: SiteQuality
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BaseQRankSum
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VQSLOD
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MQRankSum
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SIO_000300: 8.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.12e-2

QD
type: SiteQuality
SIO_000300: 1.435e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.1e-2

GenotypeDepth
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bin: 9.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.099048548426445e-5
allele num: 16396
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66262
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
allele num: 11464
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.48e-1

MQRankSum
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MQ
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VQSLOD
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BaseQRankSum
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FS
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QD
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: 1.12e-2

DP
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SIO_000300: 1.987885e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 10378
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.219660934260276e-4
allele num: 16398
num of homozygotes: 0

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

Latino
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East Asian
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.509570678099149e-5
allele num: 66244
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BaseQRankSum
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MQRankSum
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VQSLOD
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ReadPosRankSum
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QD
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FS
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InbreedingCoeff
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DP
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MQ
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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Other
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66212
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European (Finnish)
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South Asian
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VQSLOD
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BaseQRankSum
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FS
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InbreedingCoeff
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MQRankSum
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DP
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MQ
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ReadPosRankSum
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QD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66212
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.721437292865864e-5
allele num: 11466
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.972872e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.261e0

InbreedingCoeff
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SIO_000300: 9.1e-3

QD
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SIO_000300: 1.644e1

ReadPosRankSum
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SIO_000300: -2.9e-2

MQRankSum
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SIO_000300: 1.51e0

VQSLOD
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SIO_000300: -3.615e-1

ClippingRankSum
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SIO_000300: -1.25e-1

BaseQRankSum
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SIO_000300: 3.35e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11452
num of homozygotes: 0

African
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allele count: 3
allele frequency: 2.892402622445044e-4
allele num: 10372
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16364
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66106
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -5.851e-1

InbreedingCoeff
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SIO_000300: 8.0e-3

FS
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SIO_000300: 2.649e0

DP
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MQ
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ClippingRankSum
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BaseQRankSum
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SIO_000300: -1.143e0

MQRankSum
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SIO_000300: 6.46e-1

QD
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SIO_000300: 1.033e1

ReadPosRankSum
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SIO_000300: 2.34e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1854
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66140
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16378
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

FS
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SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: -1.283e0

MQ
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SIO_000300: 6.0e1

VQSLOD
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SIO_000300: -2.048e-1

MQRankSum
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SIO_000300: -1.424e0

ReadPosRankSum
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SIO_000300: 1.51e0

BaseQRankSum
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SIO_000300: 3.87e0

QD
type: SiteQuality
SIO_000300: 1.279e1

DP
type: SiteQuality
SIO_000300: 1.965401e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 13360
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GenotypeQuality
all individuals: 11497
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variant carriers: 1

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

Latino
type: Population
allele count: 1
allele frequency: 8.739730816290858e-5
allele num: 11442
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: 0
allele frequency: 0.0e0
allele num: 66034
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16356
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.159999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.629999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.47e-1

FS
type: SiteQuality
SIO_000300: 2.027e0

DP
type: SiteQuality
SIO_000300: 1.965855e6

InbreedingCoeff
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SIO_000300: 4.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 9.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

QD
type: SiteQuality
SIO_000300: 1.354e1

GenotypeDepth
all individuals: 296
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variant carriers: 11

GenotypeDepth
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variant carriers: 225

GenotypeDepth
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variant carriers: 47

GenotypeQuality
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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variant carriers: 12

GenotypeQuality
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GenotypeQuality
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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variant carriers: 13

GenotypeQuality
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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: 11

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3131
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variant carriers: 10

GenotypeQuality
all individuals: 69
bin: 1.75e1
variant carriers: 1

East Asian
type: Population
allele count: 1701
allele frequency: 1.987613928487965e-1
allele num: 8558
num of homozygotes: 185

Other
type: Population
allele count: 48
allele frequency: 5.286343612334802e-2
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 269
allele frequency: 2.588031556667308e-2
allele num: 10394
num of homozygotes: 4

European (Non-Finnish)
type: Population
allele count: 1571
allele frequency: 2.365180211375749e-2
allele num: 66422
num of homozygotes: 20

South Asian
type: Population
allele count: 910
allele frequency: 5.525197328476017e-2
allele num: 16470
num of homozygotes: 42

Latino
type: Population
allele count: 211
allele frequency: 1.837338906304424e-2
allele num: 11484
num of homozygotes: 6

European (Finnish)
type: Population
allele count: 444
allele frequency: 6.76622980798537e-2
allele num: 6562
num of homozygotes: 15

VQSLOD
type: SiteQuality
SIO_000300: 6.96e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.44e-1

MQRankSum
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SIO_000300: 1.45e-1

BaseQRankSum
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SIO_000300: -3.874e0

QD
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SIO_000300: 1.426e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.449415e6

InbreedingCoeff
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SIO_000300: 6.38e-2

MQ
type: SiteQuality
SIO_000300: 5.97e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.68e-1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66422
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.620935154897056e-5
allele num: 10394
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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MQRankSum
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SIO_000300: 1.45e-1

MQ
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SIO_000300: 5.97e1

QD
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FS
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ClippingRankSum
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SIO_000300: -1.44e-1

ReadPosRankSum
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DP
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VQSLOD
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SIO_000300: 6.96e0

InbreedingCoeff
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SIO_000300: 6.38e-2

BaseQRankSum
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SIO_000300: -3.874e0

GenotypeDepth
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variant carriers: 0

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

East Asian
type: Population
allele count: 49
allele frequency: 5.683136163303177e-3
allele num: 8622
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.510328652614487e-5
allele num: 66514
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.213150551983501e-4
allele num: 16486
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 1
allele frequency: 8.706251088281386e-5
allele num: 11486
num of homozygotes: 0

ClippingRankSum
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SIO_000300: -1.31e-1

MQRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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QD
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DP
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GenotypeDepth
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variant carriers: 1

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

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

African
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Latino
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allele frequency: 2.611420612813371e-4
allele num: 11488
num of homozygotes: 0

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

Other
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East Asian
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South Asian
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VQSLOD
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MQRankSum
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ReadPosRankSum
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MQ
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ClippingRankSum
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QD
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BaseQRankSum
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InbreedingCoeff
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DP
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SIO_000300: 2.436157e6

FS
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SIO_000300: 6.13e-1

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

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

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

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

Latino
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East Asian
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num of homozygotes: 0

European (Finnish)
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Other
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African
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South Asian
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BaseQRankSum
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MQ
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MQRankSum
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QD
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VQSLOD
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ReadPosRankSum
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FS
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InbreedingCoeff
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DP
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.004085556356645e-5
allele num: 66576
num of homozygotes: 0

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

African
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Latino
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num of homozygotes: 0

Other
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num of homozygotes: 0

East Asian
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num of homozygotes: 0

FS
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ClippingRankSum
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SIO_000300: 1.88e-1

ReadPosRankSum
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QD
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MQ
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BaseQRankSum
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DP
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MQRankSum
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SIO_000300: 3.7e-1

InbreedingCoeff
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SIO_000300: 5.999999999999999e-4

VQSLOD
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SIO_000300: 9.9e-1

GenotypeDepth
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

Other
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num of homozygotes: 0

East Asian
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allele num: 8632
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South Asian
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African
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European (Non-Finnish)
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European (Finnish)
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ClippingRankSum
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ReadPosRankSum
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FS
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MQRankSum
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VQSLOD
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DP
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BaseQRankSum
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InbreedingCoeff
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MQ
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 4.504910352283989e-5
allele num: 66594
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African
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South Asian
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Other
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East Asian
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Latino
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European (Finnish)
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ReadPosRankSum
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QD
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MQ
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ClippingRankSum
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DP
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MQRankSum
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VQSLOD
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FS
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InbreedingCoeff
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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European (Finnish)
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East Asian
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European (Non-Finnish)
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Other
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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QD
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FS
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ReadPosRankSum
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DP
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VQSLOD
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MQ
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BaseQRankSum
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variant carriers: 1514

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

GenotypeQuality
all individuals: 2540
bin: 9.25e1
variant carriers: 21

GenotypeQuality
all individuals: 2803
bin: 7.25e1
variant carriers: 6

GenotypeQuality
all individuals: 3454
bin: 8.25e1
variant carriers: 19

GenotypeQuality
all individuals: 4229
bin: 7.75e1
variant carriers: 16

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 10

European (Finnish)
type: Population
allele count: 989
allele frequency: 1.497577225923683e-1
allele num: 6604
num of homozygotes: 66

South Asian
type: Population
allele count: 2544
allele frequency: 1.541257724463831e-1
allele num: 16506
num of homozygotes: 228

European (Non-Finnish)
type: Population
allele count: 9390
allele frequency: 1.408852213053263e-1
allele num: 66650
num of homozygotes: 667

East Asian
type: Population
allele count: 735
allele frequency: 8.510884668828161e-2
allele num: 8636
num of homozygotes: 32

Latino
type: Population
allele count: 1258
allele frequency: 1.091824336052769e-1
allele num: 11522
num of homozygotes: 67

African
type: Population
allele count: 417
allele frequency: 4.00884445298981e-2
allele num: 10402
num of homozygotes: 6

Other
type: Population
allele count: 151
allele frequency: 1.662995594713656e-1
allele num: 908
num of homozygotes: 10

MQRankSum
type: SiteQuality
SIO_000300: 1.41e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.45e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

QD
type: SiteQuality
SIO_000300: 1.396e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e-1

DP
type: SiteQuality
SIO_000300: 2.906935e6

GenotypeDepth
all individuals: 506
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6184
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12542
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4553
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3326
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5501
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 64
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3566
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8421
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17087
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15886
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2163
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499880009599232e-5
allele num: 66672
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: 8642
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 9.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.127e0

QD
type: SiteQuality
SIO_000300: 1.294e1

DP
type: SiteQuality
SIO_000300: 2.424789e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.883e0

MQRankSum
type: SiteQuality
SIO_000300: 8.7e-1

FS
type: SiteQuality
SIO_000300: 1.434e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.38e-1

GenotypeDepth
all individuals: 506
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12567
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 764
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2163
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15886
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4551
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3567
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3324
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8428
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17104
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5500
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
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: 6604
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66692
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.603262755987504e-4
allele num: 11524
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.244e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -7.75e-1

DP
type: SiteQuality
SIO_000300: 2.425109e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.29e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.63e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

GenotypeDepth
all individuals: 592
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6182
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3692
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1413
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 9897
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 367
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15884
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4551
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8427
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5500
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17118
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 58
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2163
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3567
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3325
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66698
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.34e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.16e0

DP
type: SiteQuality
SIO_000300: 2.425123e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.16e0

FS
type: SiteQuality
SIO_000300: 1.025e1

MQ
type: SiteQuality
SIO_000300: 5.938e1

QD
type: SiteQuality
SIO_000300: 1.385e1

VQSLOD
type: SiteQuality
SIO_000300: -1.66e0

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

GenotypeDepth
all individuals: 449
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9899
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 506
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2224
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1829
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 987
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8434
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17161
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2161
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4552
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5497
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 3577
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15879
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3325
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 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: 1
allele frequency: 1.499115521842113e-5
allele num: 66706
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.47e1

MQRankSum
type: SiteQuality
SIO_000300: -1.315e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.14e-1

MQ
type: SiteQuality
SIO_000300: 5.913e1

VQSLOD
type: SiteQuality
SIO_000300: -6.141e-1

DP
type: SiteQuality
SIO_000300: 2.425507e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.35e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

GenotypeDepth
all individuals: 592
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 40
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 2223
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 506
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9899
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3578
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8433
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15878
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 17161
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5499
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2161
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4551
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3325
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0