20-37144950-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37144950
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37144950
    reference: chr 20
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.988C>T
  hgvsp: ENSP00000380235.3:p.His330Tyr
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.472C>T
  hgvsp: ENSP00000416646.1:p.His158Tyr
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.988C>T
  hgvsp: ENSP00000380233.1:p.His330Tyr
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.988C>T
  hgvsp: ENSP00000262879.6:p.His330Tyr
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.322C>T
  hgvsp: ENSP00000380231.1:p.His108Tyr
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.988C>T
  hgvsp: ENSP00000442959.1:p.His330Tyr
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.240C>T
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12677
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31117
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4524
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1704
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28572
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3082
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3732
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.His330Tyr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

20-37144953-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37144953
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37144953
    reference: chr 20
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.475C>G
  hgvsp: ENSP00000416646.1:p.Leu159Val
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.991C>G
  hgvsp: ENSP00000380233.1:p.Leu331Val
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.325C>G
  hgvsp: ENSP00000380231.1:p.Leu109Val
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.991C>G
  hgvsp: ENSP00000380235.3:p.Leu331Val
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.991C>G
  hgvsp: ENSP00000262879.6:p.Leu331Val
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.243C>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.991C>G
  hgvsp: ENSP00000442959.1:p.Leu331Val
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31114
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12677
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2404
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28577
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3081
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3732
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu331Val
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

20-37144972-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37144972
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37144972
    reference: chr 20
allele count: 1
allele frequency: 8.24783082049421e-6
allele num: 121244
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1010G>A
  hgvsp: ENSP00000380235.3:p.Arg337His
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1010G>A
  hgvsp: ENSP00000380233.1:p.Arg337His
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.344G>A
  hgvsp: ENSP00000380231.1:p.Arg115His
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.494G>A
  hgvsp: ENSP00000416646.1:p.Arg165His
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1010G>A
  hgvsp: ENSP00000262879.6:p.Arg337His
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1010G>A
  hgvsp: ENSP00000442959.1:p.Arg337His
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.262G>A
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30972
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12653
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2404
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4520
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg337His
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD

20-37144976-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37144976
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37144976
    reference: chr 20
allele count: 1
allele frequency: 8.249463784853985e-6
allele num: 121220
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1014C>T
  hgvsp: ENST00000397040.1:c.1014C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1014C>T
  hgvsp: ENST00000262879.6:c.1014C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1014C>T
  hgvsp: ENST00000397042.3:c.1014C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.348C>T
  hgvsp: ENST00000397038.1:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.266C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1014C>T
  hgvsp: ENST00000537204.1:c.1014C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.498C>T
  hgvsp: ENST00000438490.1:c.498C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30931
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12656
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1705
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9336
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala338Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

20-37144980-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37144980
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37144980
    reference: chr 20
allele count: 2
allele frequency: 1.651036851142517e-5
allele num: 121136
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1018C>T
  hgvsp: ENSP00000442959.1:p.Arg340Cys
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.270C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1018C>T
  hgvsp: ENSP00000380235.3:p.Arg340Cys
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1018C>T
  hgvsp: ENSP00000380233.1:p.Arg340Cys
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1018C>T
  hgvsp: ENSP00000262879.6:p.Arg340Cys
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.352C>T
  hgvsp: ENSP00000380231.1:p.Arg118Cys
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.502C>T
  hgvsp: ENSP00000416646.1:p.Arg168Cys
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12652
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30823
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2403
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3080
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28265
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg340Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum

20-37144981-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37144981
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37144981
    reference: chr 20
allele count: 2
allele frequency: 1.651145895251304e-5
allele num: 121128
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1019G>A
  hgvsp: ENSP00000380233.1:p.Arg340His
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1019G>A
  hgvsp: ENSP00000262879.6:p.Arg340His
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.271G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.353G>A
  hgvsp: ENSP00000380231.1:p.Arg118His
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1019G>A
  hgvsp: ENSP00000380235.3:p.Arg340His
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.503G>A
  hgvsp: ENSP00000416646.1:p.Arg168His
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1019G>A
  hgvsp: ENSP00000442959.1:p.Arg340His
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4518
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2403
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7268
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg340His
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: DP

20-37144993-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37144993
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37144993
    reference: chr 20
allele count: 1
allele frequency: 8.277460475126231e-6
allele num: 120810
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1031G>A
  hgvsp: ENSP00000380235.3:p.Cys344Tyr
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.515G>A
  hgvsp: ENSP00000416646.1:p.Cys172Tyr
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.283G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1031G>A
  hgvsp: ENSP00000380233.1:p.Cys344Tyr
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1031G>A
  hgvsp: ENSP00000442959.1:p.Cys344Tyr
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1031G>A
  hgvsp: ENSP00000262879.6:p.Cys344Tyr
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.365G>A
  hgvsp: ENSP00000380231.1:p.Cys122Tyr
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12591
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27809
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1704
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2403
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Cys344Tyr
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

20-37144995-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37144995
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37144995
    reference: chr 20
allele count: 1
allele frequency: 8.287338604080686e-6
allele num: 120666
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1033C>T
  hgvsp: ENST00000397040.1:c.1033C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1033C>T
  hgvsp: ENST00000262879.6:c.1033C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.285C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.517C>T
  hgvsp: ENST00000438490.1:c.517C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1033C>T
  hgvsp: ENST00000397042.3:c.1033C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.367C>T
  hgvsp: ENST00000397038.1:c.367C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1033C>T
  hgvsp: ENST00000537204.1:c.1033C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7422
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30334
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12527
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7219
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9340
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu345Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

20-37145022-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37145022
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37145022
    reference: chr 20
allele count: 4
allele frequency: 3.354241438298729e-5
allele num: 119252
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.385+9T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.303+9T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1051+9T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1051+9T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.535+9T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1051+9T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1051+9T>C
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28450
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12002
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9343
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3057
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2212
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7105
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25156
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

20-37145023-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37145023
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37145023
    reference: chr 20
allele count: 4
allele frequency: 3.354072682755036e-5
allele num: 119258
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.385+10G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1051+10G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.535+10G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1051+10G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1051+10G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1051+10G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.303+10G>A
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12006
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3059
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2225
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4502
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

20-37145035-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37145035
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37145035
    reference: chr 20
allele count: 1
allele frequency: 8.435970980259829e-6
allele num: 118540
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1051+22A>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1051+22A>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1051+22A>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.535+22A>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1051+22A>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.303+22A>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.385+22A>T
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2716
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7311
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27452
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24004
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1702
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9346
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

20-37145042-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37145042
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37145042
    reference: chr 20
allele count: 1
allele frequency: 8.450942280064228e-6
allele num: 118330
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1051+29T>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1051+29T>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.303+29T>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1051+29T>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.535+29T>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1051+29T>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.385+29T>G
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2769
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11662
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7303
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27277
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3053
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1702
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7041
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP

20-37145050-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37145050
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37145050
    reference: chr 20
allele count: 1
allele frequency: 8.490261669864665e-6
allele num: 117782
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1051+37T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.535+37T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1051+37T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1051+37T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.385+37T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.303+37T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1051+37T>C
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11597
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7296
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2670
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4496
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2504
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7024
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3727
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

20-37145053-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37145053
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37145053
    reference: chr 20
allele count: 1
allele frequency: 8.501088139281828e-6
allele num: 117632
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.535+40A>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1051+40A>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1051+40A>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.303+40A>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1051+40A>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1051+40A>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.385+40A>G
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7287
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26928
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2619
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 848
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9348
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 675
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2462
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

20-37145060-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37145060
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37145060
    reference: chr 20
allele count: 3
allele frequency: 2.564102564102564e-5
allele num: 117000
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.385+47T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1051+47T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.303+47T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1051+47T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.535+47T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1051+47T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1051+47T>C
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2364
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7289
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26872
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11574
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23097
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1703
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3723
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 633
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

20-37145063-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37145063
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37145063
    reference: chr 20
allele count: 1
allele frequency: 8.577947811765514e-6
allele num: 116578
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.385+50C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1051+50C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1051+50C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.303+50C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.535+50C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1051+50C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1051+50C>T
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26792
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7298
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1767
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22844
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2402
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 794
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP

20-37145064-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37145064
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37145064
    reference: chr 20
allele count: 3
allele frequency: 2.569637167231987e-5
allele num: 116748
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1051+51T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1051+51T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.385+51T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.535+51T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.303+51T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1051+51T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1051+51T>C
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11639
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7300
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26791
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1866
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2402
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22884
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3052
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

20-37145156-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37145156
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37145156
    reference: chr 20
allele count: 1
allele frequency: 2.247696111485727e-5
allele num: 44490
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1051+143C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1051+143C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1051+143C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.535+143C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.303+143C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.385+143C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1051+143C>T
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13333
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16004
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19774
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1511
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1144
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13725
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum

20-37145156-CAACAAATAA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37145156
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37145147
    reference: chr 20
allele count: 2
allele frequency: 4.495392222971454e-5
allele num: 44490
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13333
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19774
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16004
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31308
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13725
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1144
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1155
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4704
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: CAACAAATAA
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ

20-37145159-CAAATA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37145159
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37145154
    reference: chr 20
allele count: 3
allele frequency: 7.260406582768634e-5
allele num: 41320
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1051+152_1051+156delAAATA
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1051+152_1051+156delAAATA
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1051+152_1051+156delAAATA
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.385+152_385+156delAAATA
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.303+152_303+156delAAATA
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.535+152_535+156delAAATA
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1051+152_1051+156delAAATA
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14940
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15044
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2662
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19863
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1055
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1261
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30523
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4074
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15333
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: CAAATA
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/20-37145164-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37145164
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37145164
    reference: chr 20
allele count: 1
allele frequency: 2.927400468384075e-5
allele num: 34160
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1051+151A>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1051+151A>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.303+151A>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1051+151A>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.385+151A>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.535+151A>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1051+151A>C
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12810
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17866
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19774
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18493
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27581
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1139
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1539
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

20-37145164-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37145164
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37145164
    reference: chr 20
allele count: 1
allele frequency: 2.927400468384075e-5
allele num: 34160
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1051+151A>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.303+151A>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1051+151A>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.535+151A>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.385+151A>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1051+151A>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1051+151A>G
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17866
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12810
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19774
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1539
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum

20-37145167-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37145167
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37145167
    reference: chr 20
allele count: 1
allele frequency: 3.194479938665985e-5
allele num: 31304
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1051+154A>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1051+154A>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1051+154A>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.303+154A>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1051+154A>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.535+154A>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.385+154A>G
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11852
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19585
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19182
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1056
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2694
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 679
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1530
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 970
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26339
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19949
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/20-37145175-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37145175
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37145175
    reference: chr 20
allele count: 1
allele frequency: 4.560379423568041e-5
allele num: 21928
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1051+162A>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1051+162A>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1051+162A>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.385+162A>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1051+162A>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.535+162A>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.303+162A>C
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24500
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8649
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1712
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1382
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20863
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1202
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 815
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

20-37145183-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37145183
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37145183
    reference: chr 20
allele count: 1
allele frequency: 7.120478496154942e-5
allele num: 14044
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1051+170C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.303+170C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1051+170C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1051+170C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1051+170C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.385+170C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.535+170C>T
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14611
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28878
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5640
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29145
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1316
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15671
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

20-37145184-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37145184
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37145184
    reference: chr 20
allele count: 1
allele frequency: 7.551729346020239e-5
allele num: 13242
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.535+171G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.303+171G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.385+171G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1051+171G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1051+171G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1051+171G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1051+171G>A
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29385
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5282
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1215
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 420
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genotype quality: GenotypeQuality
  all individuals: 1710
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1075
  bin: 6.25e1
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 740
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

20-37145188-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37145188
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37145188
    reference: chr 20
allele count: 0
allele frequency: 0.0e0
allele num: 11030
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.535+175C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1051+175C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.385+175C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1051+175C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.303+175C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1051+175C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1051+175C>T
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12868
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30938
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4326
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1123
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

20-37145190-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37145190
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37145190
    reference: chr 20
allele count: 1
allele frequency: 9.900990099009902e-5
allele num: 10100
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1051+177A>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1051+177A>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1051+177A>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.385+177A>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1051+177A>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.303+177A>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.535+177A>G
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3881
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31629
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1068
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 862
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1355
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

20-37145194-A-AGC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37145194
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37145196
    reference: chr 20
allele count: 0
allele frequency: 0.0e0
allele num: 8068
alternate allele: AGC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1051+181_1051+182insGC
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1051+181_1051+182insGC
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1051+181_1051+182insGC
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.385+181_385+182insGC
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.303+181_303+182insGC
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1051+181_1051+182insGC
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.535+181_535+182insGC
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10358
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32757
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1506
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1054
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32544
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

20-37145201-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37145201
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37145201
    reference: chr 20
allele count: 0
allele frequency: 0.0e0
allele num: 6400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.535+188T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1051+188T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1051+188T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1051+188T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.385+188T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.303+188T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1051+188T>C
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33260
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8504
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 860
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1614
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS

20-37145224-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37145224
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37145224
    reference: chr 20
allele count: 0
allele frequency: 0.0e0
allele num: 2520
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1051+211G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1051+211G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.535+211G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000263473
  ensembl transcript: ENST00000583129
  gene symbol: MIR548O2
  hgvsc: ENST00000583129.1:n.19G>A
  variant of: http://identifiers.org/hgnc/41882
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1051+211G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1051+211G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.303+211G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.385+211G>A
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29225
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27652
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

20-37145248-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37145248
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37145248
    reference: chr 20
allele count: 0
allele frequency: 0.0e0
allele num: 938
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.303+235G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.385+235G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1051+235G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.535+235G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1051+235G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000263473
  ensembl transcript: ENST00000583129
  gene symbol: MIR548O2
  hgvsc: ENST00000583129.1:n.43G>A
  variant of: http://identifiers.org/hgnc/41882
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1051+235G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1051+235G>A
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19975
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 967
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2430
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17755
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

20-37145277-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37145277
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37145277
    reference: chr 20
allele count: 1
allele frequency: 1.362397820163488e-3
allele num: 734
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1051+264C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1051+264C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.385+264C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1051+264C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.535+264C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1051+264C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.303+264C>T
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13808
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11969
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

20-37145286-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37145286
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37145286
    reference: chr 20
allele count: 1
allele frequency: 1.424501424501425e-3
allele num: 702
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1051+273T>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1051+273T>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.535+273T>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1051+273T>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.385+273T>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.303+273T>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1051+273T>A
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12781
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2069
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

20-37145286-TCAAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37145286
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37145282
    reference: chr 20
allele count: 1
allele frequency: 1.424501424501425e-3
allele num: 702
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1051+278_1051+281delCAAA
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.535+278_535+281delCAAA
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1051+278_1051+281delCAAA
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.385+278_385+281delCAAA
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1051+278_1051+281delCAAA
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1051+278_1051+281delCAAA
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.303+278_303+281delCAAA
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12781
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2069
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: TCAAA
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum

20-37145298-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37145298
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37145298
    reference: chr 20
allele count: 1
allele frequency: 1.529051987767584e-3
allele num: 654
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.385+285C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1051+285C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.303+285C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.535+285C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1051+285C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1051+285C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1051+285C>T
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11972
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2664
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD

20-37145320-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37145320
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37145320
    reference: chr 20
allele count: 1
allele frequency: 1.689189189189189e-3
allele num: 592
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1051+307G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.535+307G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1051+307G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1051+307G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1051+307G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.303+307G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.385+307G>A
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11660
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 5063
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6607
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

20-37146100-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146100
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146100
    reference: chr 20
allele count: 13
allele frequency: 1.2002141920712e-4
allele num: 108314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1052-49A>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1052-49A>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.536-49A>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.386-49A>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1052-49A>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1052-49A>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.304-49A>T
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4356
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6184
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8034
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8194
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9186
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4300
  bin: 4.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 978
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2001
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2161
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 819
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1933
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 671
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1112
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1287
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4441
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

20-37146111-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146111
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146111
    reference: chr 20
allele count: 1
allele frequency: 9.20691623547609e-6
allele num: 108614
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.304-38T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1052-38T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1052-38T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1052-38T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1052-38T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.386-38T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.536-38T>C
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3661
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9790
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3033
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8676
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2520
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3076
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4723
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9525
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2198
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20170
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3726
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

20-37146118-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146118
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146118
    reference: chr 20
allele count: 2
allele frequency: 1.832005129614363e-5
allele num: 109170
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1052-31T>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1052-31T>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.536-31T>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1052-31T>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1052-31T>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.386-31T>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.304-31T>G
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9004
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10457
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10472
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4356
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6357
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4171
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3097
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4927
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/20-37146119-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146119
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146119
    reference: chr 20
allele count: 1
allele frequency: 9.151810228063111e-6
allele num: 109268
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1052-30A>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1052-30A>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.536-30A>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.304-30A>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1052-30A>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.386-30A>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1052-30A>C
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10520
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3803
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6368
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4360
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10508
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9038
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4174
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10846
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3292
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2638
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3099
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4957
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD

20-37146120-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146120
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146119
    reference: chr 20
allele count: 2
allele frequency: 1.827652380517226e-5
allele num: 109430
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.304-26delT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1052-26delT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.386-26delT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1052-26delT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1052-26delT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.536-26delT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1052-26delT
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10608
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3774
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4364
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9070
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6380
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 528
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3361
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2078
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2651
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1927
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: AT
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum

20-37146120-ATTTCATT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146120
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146113
    reference: chr 20
allele count: 3
allele frequency: 2.741478570775839e-5
allele num: 109430
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1052-27_1052-21delTTCATTT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1052-27_1052-21delTTCATTT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.304-27_304-21delTTCATTT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.536-27_536-21delTTCATTT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1052-27_1052-21delTTCATTT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1052-27_1052-21delTTCATTT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.386-27_386-21delTTCATTT
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3774
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4364
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9070
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10608
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6380
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20194
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3361
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2651
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1927
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2078
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: ATTTCATT
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD

20-37146121-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146121
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146121
    reference: chr 20
allele count: 1
allele frequency: 9.124587112433163e-6
allele num: 109594
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1052-28T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.386-28T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1052-28T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.536-28T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1052-28T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.304-28T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1052-28T>C
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 10556
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3765
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3054
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6390
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9101
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4359
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5003
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3824
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4192
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 572
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

20-37146127-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146127
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146127
    reference: chr 20
allele count: 1
allele frequency: 9.056330374932077e-6
allele num: 110420
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1052-22T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1052-22T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.304-22T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1052-22T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.386-22T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1052-22T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.536-22T>C
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9307
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3566
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10449
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6469
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4396
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3071
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10952
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11388
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4246
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3479
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2097
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

20-37146131-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146131
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146132
    reference: chr 20
allele count: 3411
allele frequency: 4.579629977712736e-2
allele num: 74482
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.386-4dupT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1052-4dupT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1052-4dupT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1052-4dupT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1052-4dupT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.304-4dupT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.536-4dupT
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 7.5e0
  variant carriers: 252
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 7.25e1
  variant carriers: 158
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 6.75e1
  variant carriers: 204
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 9.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 6677
  bin: 4.25e1
  variant carriers: 689
genotype depth: GenotypeDepth
  all individuals: 5973
  bin: 3.75e1
  variant carriers: 633
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 1.75e1
  variant carriers: 112
genotype depth: GenotypeDepth
  all individuals: 5468
  bin: 5.25e1
  variant carriers: 495
genotype depth: GenotypeDepth
  all individuals: 2691
  bin: 1.25e1
  variant carriers: 347
genotype depth: GenotypeDepth
  all individuals: 3986
  bin: 9.75e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 4436
  bin: 5.75e1
  variant carriers: 371
genotype depth: GenotypeDepth
  all individuals: 4497
  bin: 3.25e1
  variant carriers: 561
genotype depth: GenotypeDepth
  all individuals: 2923
  bin: 2.75e1
  variant carriers: 381
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 2.25e1
  variant carriers: 246
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 7.75e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 3497
  bin: 6.25e1
  variant carriers: 277
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 8.25e1
  variant carriers: 103
genotype depth: GenotypeDepth
  all individuals: 6236
  bin: 4.75e1
  variant carriers: 596
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 8.75e1
  variant carriers: 49
genotype quality: GenotypeQuality
  all individuals: 3116
  bin: 1.75e1
  variant carriers: 473
genotype quality: GenotypeQuality
  all individuals: 1639
  bin: 6.75e1
  variant carriers: 153
genotype quality: GenotypeQuality
  all individuals: 8211
  bin: 9.75e1
  variant carriers: 340
genotype quality: GenotypeQuality
  all individuals: 1132
  bin: 8.25e1
  variant carriers: 70
genotype quality: GenotypeQuality
  all individuals: 2027
  bin: 5.25e1
  variant carriers: 226
genotype quality: GenotypeQuality
  all individuals: 3385
  bin: 1.25e1
  variant carriers: 523
genotype quality: GenotypeQuality
  all individuals: 2305
  bin: 4.75e1
  variant carriers: 310
genotype quality: GenotypeQuality
  all individuals: 11883
  bin: 2.5e0
  variant carriers: 463
genotype quality: GenotypeQuality
  all individuals: 3529
  bin: 2.25e1
  variant carriers: 428
genotype quality: GenotypeQuality
  all individuals: 3018
  bin: 2.75e1
  variant carriers: 389
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum

20-37146131-C-CTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146131
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146133
    reference: chr 20
allele count: 18
allele frequency: 2.4166912811149e-4
allele num: 74482
alternate allele: CTT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1052-5_1052-4dupTT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1052-5_1052-4dupTT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.536-5_536-4dupTT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1052-5_1052-4dupTT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.386-5_386-4dupTT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1052-5_1052-4dupTT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.304-5_304-4dupTT
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5468
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2923
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2691
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4436
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5973
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6677
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4497
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3497
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3986
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8211
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3385
  bin: 1.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 2116
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2649
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2804
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2027
  bin: 5.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3116
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1132
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11883
  bin: 2.5e0
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 2305
  bin: 4.75e1
  variant carriers: 2
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

20-37146131-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146131
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146130
    reference: chr 20
allele count: 19118
allele frequency: 2.566794661797481e-1
allele num: 74482
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1052-4delT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.304-4delT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1052-4delT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.536-4delT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.386-4delT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1052-4delT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1052-4delT
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 9.25e1
  variant carriers: 225
genotype depth: GenotypeDepth
  all individuals: 4436
  bin: 5.75e1
  variant carriers: 1961
genotype depth: GenotypeDepth
  all individuals: 2923
  bin: 2.75e1
  variant carriers: 1212
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 7.5e0
  variant carriers: 348
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 8.75e1
  variant carriers: 297
genotype depth: GenotypeDepth
  all individuals: 3497
  bin: 6.25e1
  variant carriers: 1594
genotype depth: GenotypeDepth
  all individuals: 4497
  bin: 3.25e1
  variant carriers: 2105
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 2.25e1
  variant carriers: 539
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 8.25e1
  variant carriers: 468
genotype depth: GenotypeDepth
  all individuals: 6677
  bin: 4.25e1
  variant carriers: 3129
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 1.75e1
  variant carriers: 322
genotype depth: GenotypeDepth
  all individuals: 5468
  bin: 5.25e1
  variant carriers: 2368
genotype depth: GenotypeDepth
  all individuals: 2691
  bin: 1.25e1
  variant carriers: 594
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 6.75e1
  variant carriers: 1126
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 7.75e1
  variant carriers: 627
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 7.25e1
  variant carriers: 853
genotype depth: GenotypeDepth
  all individuals: 6236
  bin: 4.75e1
  variant carriers: 2758
genotype depth: GenotypeDepth
  all individuals: 5973
  bin: 3.75e1
  variant carriers: 2889
genotype depth: GenotypeDepth
  all individuals: 3986
  bin: 9.75e1
  variant carriers: 618
genotype quality: GenotypeQuality
  all individuals: 984
  bin: 8.75e1
  variant carriers: 584
genotype quality: GenotypeQuality
  all individuals: 11883
  bin: 2.5e0
  variant carriers: 1079
genotype quality: GenotypeQuality
  all individuals: 2436
  bin: 4.25e1
  variant carriers: 1056
genotype quality: GenotypeQuality
  all individuals: 3018
  bin: 2.75e1
  variant carriers: 1161
genotype quality: GenotypeQuality
  all individuals: 2305
  bin: 4.75e1
  variant carriers: 1022
genotype quality: GenotypeQuality
  all individuals: 3529
  bin: 2.25e1
  variant carriers: 1203
genotype quality: GenotypeQuality
  all individuals: 1264
  bin: 7.75e1
  variant carriers: 694
genotype quality: GenotypeQuality
  all individuals: 1390
  bin: 7.25e1
  variant carriers: 739
genotype quality: GenotypeQuality
  all individuals: 2649
  bin: 3.75e1
  variant carriers: 1057
genotype quality: GenotypeQuality
  all individuals: 3385
  bin: 1.25e1
  variant carriers: 1199
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: CT
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

20-37146131-CTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146131
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146129
    reference: chr 20
allele count: 95
allele frequency: 1.275475953921753e-3
allele num: 74482
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.304-5_304-4delTT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.386-5_386-4delTT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1052-5_1052-4delTT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1052-5_1052-4delTT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1052-5_1052-4delTT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.536-5_536-4delTT
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1052-5_1052-4delTT
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5973
  bin: 3.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 2.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6677
  bin: 4.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 6236
  bin: 4.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2923
  bin: 2.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 4436
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5468
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 4497
  bin: 3.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3497
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2691
  bin: 1.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3986
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 6.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2116
  bin: 6.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2305
  bin: 4.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 2804
  bin: 3.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 2649
  bin: 3.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 2027
  bin: 5.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 863
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3529
  bin: 2.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 3116
  bin: 1.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 3385
  bin: 1.25e1
  variant carriers: 23
genotype quality: GenotypeQuality
  all individuals: 3018
  bin: 2.75e1
  variant carriers: 14
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: CTT
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

20-37146131-CTTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146131
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146128
    reference: chr 20
allele count: 206
allele frequency: 2.765768910609275e-3
allele num: 74482
alternate allele: C
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5973
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4436
  bin: 5.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 6677
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5468
  bin: 5.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 7.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 6.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 2923
  bin: 2.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2691
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 4497
  bin: 3.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 6236
  bin: 4.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 3986
  bin: 9.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 7.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3497
  bin: 6.25e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 984
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3018
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1802
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2649
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3385
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2027
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8211
  bin: 9.75e1
  variant carriers: 197
genotype quality: GenotypeQuality
  all individuals: 2116
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3887
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2436
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2305
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3116
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11883
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1639
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2804
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3529
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1132
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 863
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1390
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1264
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 4
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4088
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 554
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 1
  allele frequency: 1.381978993919292e-4
  allele num: 7236
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 3
  allele frequency: 3.719315645921151e-4
  allele num: 8066
  num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: CTTT
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

20-37146138-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146138
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146138
    reference: chr 20
allele count: 1
allele frequency: 8.654412019247412e-6
allele num: 115548
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1052-11T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1052-11T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.386-11T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.536-11T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1052-11T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1052-11T>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.304-11T>C
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6899
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2663
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3297
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4750
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7129
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5991
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4566
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6079
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3079
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 665
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2544
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1847
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 810
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 876
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3011
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2666
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35173
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

20-37146142-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146142
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146142
    reference: chr 20
allele count: 1
allele frequency: 8.639905997822744e-6
allele num: 115742
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1052-7T>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.304-7T>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.536-7T>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1052-7T>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1052-7T>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1052-7T>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.386-7T>A
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3323
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3299
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6898
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5991
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4575
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2757
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6083
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4749
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3079
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1849
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 595
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2668
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2061
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3011
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 3.75e1
  variant carriers: 0
hgvs: c.1052-7T>A
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

20-37146146-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146146
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146146
    reference: chr 20
allele count: 4
allele frequency: 3.472704542297541e-5
allele num: 115184
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1052-3A>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.386-3A>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1052-3A>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.536-3A>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1052-3A>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1052-3A>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.304-3A>T
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3371
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6097
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6909
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1907
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3296
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5994
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4753
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3078
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7138
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1868
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2677
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2765
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35161
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 586
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
hgvs: c.1052-3A>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/20-37146160-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146160
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146160
    reference: chr 20
allele count: 1
allele frequency: 8.461811843151855e-6
allele num: 118178
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.547C>A
  hgvsp: ENSP00000416646.1:p.Pro183Thr
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.397C>A
  hgvsp: ENSP00000380231.1:p.Pro133Thr
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1063C>A
  hgvsp: ENSP00000380233.1:p.Pro355Thr
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1063C>A
  hgvsp: ENSP00000442959.1:p.Pro355Thr
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1063C>A
  hgvsp: ENSP00000380235.3:p.Pro355Thr
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.315C>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1063C>A
  hgvsp: ENSP00000262879.6:p.Pro355Thr
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2788
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6093
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6906
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5998
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3108
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2100
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1961
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro355Thr
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

20-37146162-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146162
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146162
    reference: chr 20
allele count: 1
allele frequency: 8.42800795603951e-6
allele num: 118652
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.399C>T
  hgvsp: ENST00000397038.1:c.399C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1065C>T
  hgvsp: ENST00000537204.1:c.1065C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1065C>T
  hgvsp: ENST00000262879.6:c.1065C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.549C>T
  hgvsp: ENST00000438490.1:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.317C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1065C>T
  hgvsp: ENST00000397042.3:c.1065C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1065C>T
  hgvsp: ENST00000397040.1:c.1065C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2909
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4752
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3424
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6092
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6904
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5998
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1689
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35267
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2846
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Pro355Pro
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD

20-37146164-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146164
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146164
    reference: chr 20
allele count: 1
allele frequency: 8.395882659143956e-6
allele num: 119106
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1067G>A
  hgvsp: ENSP00000380233.1:p.Arg356Gln
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1067G>A
  hgvsp: ENSP00000442959.1:p.Arg356Gln
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1067G>A
  hgvsp: ENSP00000262879.6:p.Arg356Gln
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1067G>A
  hgvsp: ENSP00000380235.3:p.Arg356Gln
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.551G>A
  hgvsp: ENSP00000416646.1:p.Arg184Gln
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.401G>A
  hgvsp: ENSP00000380231.1:p.Arg134Gln
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.319G>A
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6091
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6902
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3587
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3958
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3071
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4632
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3012
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4750
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2061
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2851
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1350
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg356Gln
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

20-37146169-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146169
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146169
    reference: chr 20
allele count: 1
allele frequency: 8.348081610845828e-6
allele num: 119788
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.556G>A
  hgvsp: ENSP00000416646.1:p.Asp186Asn
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1072G>A
  hgvsp: ENSP00000380235.3:p.Asp358Asn
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.406G>A
  hgvsp: ENSP00000380231.1:p.Asp136Asn
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1072G>A
  hgvsp: ENSP00000380233.1:p.Asp358Asn
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1072G>A
  hgvsp: ENSP00000442959.1:p.Asp358Asn
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1072G>A
  hgvsp: ENSP00000262879.6:p.Asp358Asn
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.324G>A
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3655
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6092
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6904
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3203
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4646
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3071
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4481
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4750
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35273
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2102
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3367
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7291
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp358Asn
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

20-37146173-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146173
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146173
    reference: chr 20
allele count: 1
allele frequency: 8.323068215867098e-6
allele num: 120148
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1076G>C
  hgvsp: ENSP00000262879.6:p.Ser359Thr
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1076G>C
  hgvsp: ENSP00000380233.1:p.Ser359Thr
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1076G>C
  hgvsp: ENSP00000442959.1:p.Ser359Thr
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1076G>C
  hgvsp: ENSP00000380235.3:p.Ser359Thr
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.328G>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.560G>C
  hgvsp: ENSP00000416646.1:p.Ser187Thr
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.410G>C
  hgvsp: ENSP00000380231.1:p.Ser137Thr
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6904
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4651
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3705
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3342
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3071
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4750
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6094
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 712
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3056
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2125
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2119
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser359Thr
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

20-37146177-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146177
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146177
    reference: chr 20
allele count: 1
allele frequency: 8.304958059961797e-6
allele num: 120410
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1080T>A
  hgvsp: ENST00000262879.6:c.1080T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1080T>A
  hgvsp: ENST00000397042.3:c.1080T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.332T>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1080T>A
  hgvsp: ENST00000537204.1:c.1080T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.414T>A
  hgvsp: ENST00000397038.1:c.414T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.564T>A
  hgvsp: ENST00000438490.1:c.564T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1080T>A
  hgvsp: ENST00000397040.1:c.1080T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3525
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6905
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7154
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4655
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6096
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3071
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5998
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2889
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3486
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7757
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala360Ala
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ

20-37146180-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146180
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146180
    reference: chr 20
allele count: 13
allele frequency: 1.078015125381452e-4
allele num: 120592
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.417C>G
  hgvsp: ENST00000397038.1:c.417C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.335C>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1083C>G
  hgvsp: ENST00000262879.6:c.1083C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.567C>G
  hgvsp: ENST00000438490.1:c.567C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1083C>G
  hgvsp: ENST00000397042.3:c.1083C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1083C>G
  hgvsp: ENST00000397040.1:c.1083C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1083C>G
  hgvsp: ENST00000537204.1:c.1083C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6903
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5998
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3075
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3303
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4750
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6093
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4657
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3536
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2884
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3057
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro361Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

20-37146183-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146183
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146183
    reference: chr 20
allele count: 2
allele frequency: 1.655711376392867e-5
allele num: 120794
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1086A>G
  hgvsp: ENST00000397042.3:c.1086A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1086A>G
  hgvsp: ENST00000537204.1:c.1086A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.570A>G
  hgvsp: ENST00000438490.1:c.570A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1086A>G
  hgvsp: ENST00000262879.6:c.1086A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.420A>G
  hgvsp: ENST00000397038.1:c.420A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.338A>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1086A>G
  hgvsp: ENST00000397040.1:c.1086A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3723
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5998
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6903
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4717
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6096
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4661
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2924
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3559
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro362Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP

20-37146189-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146189
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146189
    reference: chr 20
allele count: 29
allele frequency: 2.396139736259378e-4
allele num: 121028
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.426C>T
  hgvsp: ENST00000397038.1:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1092C>T
  hgvsp: ENST00000262879.6:c.1092C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1092C>T
  hgvsp: ENST00000397042.3:c.1092C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.576C>T
  hgvsp: ENST00000438490.1:c.576C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.344C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1092C>T
  hgvsp: ENST00000397040.1:c.1092C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1092C>T
  hgvsp: ENST00000537204.1:c.1092C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4664
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6098
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 9.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7158
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6902
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4749
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3828
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4793
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2152
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3061
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro364Pro
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff

20-37146198-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146198
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146198
    reference: chr 20
allele count: 1
allele frequency: 8.249599894405122e-6
allele num: 121218
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.353A>G
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.435A>G
  hgvsp: ENST00000397038.1:c.435A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1101A>G
  hgvsp: ENST00000262879.6:c.1101A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1101A>G
  hgvsp: ENST00000397040.1:c.1101A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1101A>G
  hgvsp: ENST00000537204.1:c.1101A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1101A>G
  hgvsp: ENST00000397042.3:c.1101A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.585A>G
  hgvsp: ENST00000438490.1:c.585A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6093
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3882
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6903
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3061
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2167
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8496
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg367Arg
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

20-37146203-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146203
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146203
    reference: chr 20
allele count: 1
allele frequency: 8.246334504312833e-6
allele num: 121266
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1106G>A
  hgvsp: ENSP00000380235.3:p.Ser369Asn
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1106G>A
  hgvsp: ENSP00000262879.6:p.Ser369Asn
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1106G>A
  hgvsp: ENSP00000442959.1:p.Ser369Asn
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1106G>A
  hgvsp: ENSP00000380233.1:p.Ser369Asn
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.440G>A
  hgvsp: ENSP00000380231.1:p.Ser147Asn
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.590G>A
  hgvsp: ENSP00000416646.1:p.Ser197Asn
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.358G>A
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6902
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6093
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3899
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3600
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2883
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2169
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser369Asn
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/20-37146212-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146212
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146212
    reference: chr 20
allele count: 3
allele frequency: 2.472799208704253e-5
allele num: 121320
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1115A>C
  hgvsp: ENSP00000380235.3:p.Gln372Pro
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.599A>C
  hgvsp: ENSP00000416646.1:p.Gln200Pro
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1115A>C
  hgvsp: ENSP00000442959.1:p.Gln372Pro
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1115A>C
  hgvsp: ENSP00000262879.6:p.Gln372Pro
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.449A>C
  hgvsp: ENSP00000380231.1:p.Gln150Pro
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1115A>C
  hgvsp: ENSP00000380233.1:p.Gln372Pro
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.367A>C
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3074
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4896
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6094
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6900
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5998
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3846
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4667
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3303
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2883
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2127
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3616
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gln372Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/20-37146232-A-AC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146232
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146233
    reference: chr 20
allele count: 121
allele frequency: 9.989597609101266e-4
allele num: 121126
alternate allele: AC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.394dupC
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1142dupC
  hgvsp: ENSP00000380235.3:p.His382ThrfsTer2
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1142dupC
  hgvsp: ENSP00000442959.1:p.His382ThrfsTer2
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1142dupC
  hgvsp: ENSP00000380233.1:p.His382ThrfsTer2
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1142dupC
  hgvsp: ENSP00000262879.6:p.His382ThrfsTer2
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.476dupC
  hgvsp: ENSP00000380231.1:p.His160ThrfsTer2
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.626dupC
  hgvsp: ENSP00000416646.1:p.His210ThrfsTer2
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4843
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6095
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6900
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3851
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4677
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3110
  bin: 9.75e1
  variant carriers: 122
genotype depth: GenotypeDepth
  all individuals: 4747
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3061
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2167
  bin: 7.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 2941
  bin: 7.75e1
  variant carriers: 7
hgvs: p.His382ThrfsTer2
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

20-37146237-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146237
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146237
    reference: chr 20
allele count: 16
allele frequency: 1.318478475838882e-4
allele num: 121352
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1140C>G
  hgvsp: ENST00000397042.3:c.1140C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1140C>G
  hgvsp: ENST00000537204.1:c.1140C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.624C>G
  hgvsp: ENST00000438490.1:c.624C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1140C>G
  hgvsp: ENST00000262879.6:c.1140C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1140C>G
  hgvsp: ENST00000397040.1:c.1140C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.474C>G
  hgvsp: ENST00000397038.1:c.474C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.392C>G
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6093
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4750
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4670
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5996
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7159
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6903
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4831
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3851
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3969
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3052
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2935
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2883
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Pro380Pro
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

20-37146237-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146237
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146237
    reference: chr 20
allele count: 5
allele frequency: 4.120245236996506e-5
allele num: 121352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.392C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.474C>T
  hgvsp: ENST00000397038.1:c.474C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.624C>T
  hgvsp: ENST00000438490.1:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1140C>T
  hgvsp: ENST00000397042.3:c.1140C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1140C>T
  hgvsp: ENST00000262879.6:c.1140C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1140C>T
  hgvsp: ENST00000537204.1:c.1140C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1140C>T
  hgvsp: ENST00000397040.1:c.1140C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5996
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6903
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3969
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4750
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3851
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4831
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4670
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6093
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3052
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2935
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2116
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro380Pro
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/20-37146239-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146239
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146239
    reference: chr 20
allele count: 3
allele frequency: 2.472147142197904e-5
allele num: 121352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.394C>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1142C>A
  hgvsp: ENSP00000262879.6:p.Pro381Gln
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1142C>A
  hgvsp: ENSP00000380235.3:p.Pro381Gln
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1142C>A
  hgvsp: ENSP00000442959.1:p.Pro381Gln
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.476C>A
  hgvsp: ENSP00000380231.1:p.Pro159Gln
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1142C>A
  hgvsp: ENSP00000380233.1:p.Pro381Gln
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.626C>A
  hgvsp: ENSP00000416646.1:p.Pro209Gln
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4747
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6905
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5996
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4668
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6095
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2252
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3610
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35336
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro381Gln
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

20-37146239-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146239
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146239
    reference: chr 20
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.394C>T
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1142C>T
  hgvsp: ENSP00000262879.6:p.Pro381Leu
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1142C>T
  hgvsp: ENSP00000380235.3:p.Pro381Leu
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1142C>T
  hgvsp: ENSP00000380233.1:p.Pro381Leu
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.626C>T
  hgvsp: ENSP00000416646.1:p.Pro209Leu
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.476C>T
  hgvsp: ENSP00000380231.1:p.Pro159Leu
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1142C>T
  hgvsp: ENSP00000442959.1:p.Pro381Leu
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5996
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6095
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4668
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6905
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4747
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2151
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2114
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro381Leu
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/20-37146244-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146244
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146244
    reference: chr 20
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.399A>C
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1147A>C
  hgvsp: ENSP00000380233.1:p.Asn383His
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.481A>C
  hgvsp: ENSP00000380231.1:p.Asn161His
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1147A>C
  hgvsp: ENSP00000442959.1:p.Asn383His
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.631A>C
  hgvsp: ENSP00000416646.1:p.Asn211His
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1147A>C
  hgvsp: ENSP00000262879.6:p.Asn383His
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1147A>C
  hgvsp: ENSP00000380235.3:p.Asn383His
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3859
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6097
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4748
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6906
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3963
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 35335
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3606
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3055
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2152
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2114
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asn383His
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

20-37146249-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37146249
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 37146249
    reference: chr 20
allele count: 4
allele frequency: 3.296196189597204e-5
allele num: 121352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380235
  ensembl transcript: ENST00000397042
  gene symbol: RALGAPB
  hgvsc: ENST00000397042.3:c.1152G>A
  hgvsp: ENST00000397042.3:c.1152G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380231
  ensembl transcript: ENST00000397038
  gene symbol: RALGAPB
  hgvsc: ENST00000397038.1:c.486G>A
  hgvsp: ENST00000397038.1:c.486G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000442959
  ensembl transcript: ENST00000537204
  gene symbol: RALGAPB
  hgvsc: ENST00000537204.1:c.1152G>A
  hgvsp: ENST00000537204.1:c.1152G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000416646
  ensembl transcript: ENST00000438490
  gene symbol: RALGAPB
  hgvsc: ENST00000438490.1:c.636G>A
  hgvsp: ENST00000438490.1:c.636G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170471
  ensembl transcript: ENST00000461423
  gene symbol: RALGAPB
  hgvsc: ENST00000461423.1:n.404G>A
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000262879
  ensembl transcript: ENST00000262879
  gene symbol: RALGAPB
  hgvsc: ENST00000262879.6:c.1152G>A
  hgvsp: ENST00000262879.6:c.1152G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170471
  ensembl protein: ENSP00000380233
  ensembl transcript: ENST00000397040
  gene symbol: RALGAPB
  hgvsc: ENST00000397040.1:c.1152G>A
  hgvsp: ENST00000397040.1:c.1152G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29221
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4818
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6905
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7161
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6097
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3856
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3969
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg384Arg
num of homozygotes: 0
reference allele: G

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

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

GenotypeQuality
all individuals: 2404
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9333
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7311
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 1.036e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.83e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -8.712999999999999e0

DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.22e1

ClippingRankSum
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SIO_000300: 1.25e0

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
all individuals: 7311
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

QD
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.493e0

MQRankSum
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SIO_000300: 2.04e0

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -1.058e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -5.3e-1

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499790029395885e-5
allele num: 66676
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16412
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.743581e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.528e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 3.71e-1

MQ
type: SiteQuality
SIO_000300: 5.922e1

FS
type: SiteQuality
SIO_000300: 4.87e-1

QD
type: SiteQuality
SIO_000300: 1.269e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499970000599988e-5
allele num: 66668
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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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 count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.743553e6

BaseQRankSum
type: SiteQuality
SIO_000300: -9.18e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.77e-1

ReadPosRankSum
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QD
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SIO_000300: 1.208e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.535e0

FS
type: SiteQuality
SIO_000300: 4.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 6.49e-1

MQ
type: SiteQuality
SIO_000300: 5.935e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

African
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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: 2
allele frequency: 1.224289911851126e-4
allele num: 16336
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DP
type: SiteQuality
SIO_000300: 1.742681e6

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.11e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

FS
type: SiteQuality
SIO_000300: 1.856e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.95e-1

QD
type: SiteQuality
SIO_000300: 1.198e1

MQRankSum
type: SiteQuality
SIO_000300: -4.72e-1

GenotypeQuality
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variant carriers: 0

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

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

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

African
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allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16334
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
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VQSLOD
type: SiteQuality
SIO_000300: 2.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.15e-1

InbreedingCoeff
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SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
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ReadPosRankSum
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.24e-1

MQ
type: SiteQuality
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16088
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502087902184036e-5
allele num: 66574
num of homozygotes: 0

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

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

VQSLOD
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ClippingRankSum
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MQRankSum
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QD
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 4.63e-1

InbreedingCoeff
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DP
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ReadPosRankSum
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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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: 1
allele frequency: 1.502629601803156e-5
allele num: 66550
num of homozygotes: 0

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

Other
type: Population
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East Asian
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South Asian
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FS
type: SiteQuality
SIO_000300: 5.811e0

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

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

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

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

European (Non-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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allele frequency: 3.458412588621823e-4
allele num: 11566
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South Asian
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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East Asian
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Other
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MQ
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BaseQRankSum
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ReadPosRankSum
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FS
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ClippingRankSum
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QD
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VQSLOD
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InbreedingCoeff
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MQRankSum
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DP
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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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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3052
bin: 7.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.157407407407407e-4
allele num: 8640
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14408
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.985e0

MQ
type: SiteQuality
SIO_000300: 5.986e1

MQRankSum
type: SiteQuality
SIO_000300: -1.91e-1

FS
type: SiteQuality
SIO_000300: 2.095e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

DP
type: SiteQuality
SIO_000300: 1.690576e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.52e-1

QD
type: SiteQuality
SIO_000300: 1.392e1

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2735
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2403
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4500
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3724
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9346
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23850
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 765
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515151515151515e-5
allele num: 66000
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14264
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.75e-1

FS
type: SiteQuality
SIO_000300: 3.516e0

QD
type: SiteQuality
SIO_000300: 1.627e1

VQSLOD
type: SiteQuality
SIO_000300: 6.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.988e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.75e-1

DP
type: SiteQuality
SIO_000300: 1.6874e6

GenotypeQuality
all individuals: 858
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2403
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23458
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3053
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1702
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9347
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 97
bin: 4.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
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: 10364
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13848
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517865274278255e-5
allele num: 65882
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 9.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.71e-1

FS
type: SiteQuality
SIO_000300: 3.924e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

QD
type: SiteQuality
SIO_000300: 1.822e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.0e0

VQSLOD
type: SiteQuality
SIO_000300: -7.462e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

DP
type: SiteQuality
SIO_000300: 1.682608e6

GenotypeQuality
all individuals: 230
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7023
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1702
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4497
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23433
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2402
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3052
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3726
bin: 8.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
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: 1.518602885345482e-5
allele num: 65850
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13726
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.596e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.57e0

VQSLOD
type: SiteQuality
SIO_000300: 2.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.7e-2

DP
type: SiteQuality
SIO_000300: 1.681726e6

MQRankSum
type: SiteQuality
SIO_000300: 8.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.454e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

QD
type: SiteQuality
SIO_000300: 1.681e1

GenotypeQuality
all individuals: 2101
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 844
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6985
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4493
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3049
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2402
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9353
bin: 9.75e1
variant carriers: 3

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13270
num of homozygotes: 0

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

East Asian
type: Population
allele count: 3
allele frequency: 3.477857639693948e-4
allele num: 8626
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65726
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.679919e6

VQSLOD
type: SiteQuality
SIO_000300: -1.889e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

MQ
type: SiteQuality
SIO_000300: 5.979e1

QD
type: SiteQuality
SIO_000300: 2.991e1

MQRankSum
type: SiteQuality
SIO_000300: -6.830000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.45e-1

FS
type: SiteQuality
SIO_000300: 3.372e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e-1

GenotypeQuality
all individuals: 1703
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6980
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4491
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3724
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 835
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 618
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3051
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9352
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.678668215253581e-5
allele num: 10332
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13014
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65586
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

VQSLOD
type: SiteQuality
SIO_000300: -3.196e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.93e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.427e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.66e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

QD
type: SiteQuality
SIO_000300: 1.143e1

DP
type: SiteQuality
SIO_000300: 1.680242e6

GenotypeQuality
all individuals: 466
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9355
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 622
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 719
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1703
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6982
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4491
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3727
bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 2.287282708142727e-4
allele num: 13116
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65640
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: 10336
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.641e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.25e-1

FS
type: SiteQuality
SIO_000300: 3.38e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

DP
type: SiteQuality
SIO_000300: 1.680418e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.72e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 125
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31308
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4704
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1155
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 911
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4210
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4186
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2950
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4036
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.013485310643763e-5
allele num: 24916
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3794
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 398
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.44e-1

FS
type: SiteQuality
SIO_000300: 2.897e0

QD
type: SiteQuality
SIO_000300: 9.630000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.63e-2

DP
type: SiteQuality
SIO_000300: 5.51944e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

MQ
type: SiteQuality
SIO_000300: 5.113e1

MQRankSum
type: SiteQuality
SIO_000300: -2.793e0

GenotypeQuality
all individuals: 1511
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 911
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 108
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4036
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4210
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 8.026970621287526e-5
allele num: 24916
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4186
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 398
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2950
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3794
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

QD
type: SiteQuality
SIO_000300: 9.630000000000001e0

DP
type: SiteQuality
SIO_000300: 5.51944e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.63e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.793e0

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

FS
type: SiteQuality
SIO_000300: 2.897e0

MQ
type: SiteQuality
SIO_000300: 5.113e1

GenotypeQuality
all individuals: 64
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1145
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 849
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 88
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 1.295784381478922e-4
allele num: 23152
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3658
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 358
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3936
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3946
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2694
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.036e0

VQSLOD
type: SiteQuality
SIO_000300: 3.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.07e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.96e-1

MQ
type: SiteQuality
SIO_000300: 5.018e1

MQRankSum
type: SiteQuality
SIO_000300: -1.953e0

QD
type: SiteQuality
SIO_000300: 1.207e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

DP
type: SiteQuality
SIO_000300: 5.16817e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.0e-2

GenotypeQuality
all individuals: 632
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 19048
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.531073446327684e-4
allele num: 2832
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3168
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 312
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3320
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3376
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2104
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.36e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.16e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

DP
type: SiteQuality
SIO_000300: 4.61077e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.15e0

VQSLOD
type: SiteQuality
SIO_000300: 2.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.67e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.348e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

GenotypeQuality
all individuals: 1139
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3057
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 19048
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 312
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2104
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.962085308056872e-4
allele num: 3376
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3168
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2832
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3320
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.348e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

VQSLOD
type: SiteQuality
SIO_000300: 2.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.67e-1

DP
type: SiteQuality
SIO_000300: 4.61077e5

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.16e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.36e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.15e0

GenotypeQuality
all individuals: 265
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 53
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 333
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GenotypeQuality
all individuals: 61
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1898
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2984
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.759705103098721e-5
allele num: 17362
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3104
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2504
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3152
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 300
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.86e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.37968e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.93e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.79e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.26e-2

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e0

QD
type: SiteQuality
SIO_000300: 1.499e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 10
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variant carriers: 1

GenotypeQuality
all individuals: 154
bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 8.207485226526592e-5
allele num: 12184
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2352
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2056
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1236
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2326
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.06e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.067e0

DP
type: SiteQuality
SIO_000300: 3.57121e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.42e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.792e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.99e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.242e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.99e-1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 7
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variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1364
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1560
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.119951040391676e-4
allele num: 1634
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 140
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7826
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.90632e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.279e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

VQSLOD
type: SiteQuality
SIO_000300: 4.08e0

GenotypeQuality
all individuals: 15206
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29580
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GenotypeQuality
all individuals: 7
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variant carriers: 1

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 142
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 101
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GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1464
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.510574018126888e-3
allele num: 662
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1522
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1312
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 752
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7398
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.337e0

QD
type: SiteQuality
SIO_000300: 9.41e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.710000000000001e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e0

MQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.01e-1

DP
type: SiteQuality
SIO_000300: 2.82886e5

GenotypeQuality
all individuals: 2
bin: 9.25e1
variant carriers: 1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1280
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1088
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1294
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6160
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 112
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 486
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

DP
type: SiteQuality
SIO_000300: 2.57531e5

QD
type: SiteQuality
SIO_000300: 9.07e0

VQSLOD
type: SiteQuality
SIO_000300: -2.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.049999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 9.56e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 115
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 110
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1002
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.785076758300607e-4
allele num: 5602
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1202
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1190
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 552
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 442
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.365e0

DP
type: SiteQuality
SIO_000300: 2.45781e5

BaseQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.149999999999999e-2

MQ
type: SiteQuality
SIO_000300: 5.907e1

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.64e0

QD
type: SiteQuality
SIO_000300: 1.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.638e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 21
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GenotypeQuality
all individuals: 677
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1008
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1026
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 418
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4398
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.712e1

VQSLOD
type: SiteQuality
SIO_000300: -6.747e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.630000000000001e-2

DP
type: SiteQuality
SIO_000300: 2.19482e5

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.56e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.92e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.221e0

QD
type: SiteQuality
SIO_000300: 5.67e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7890
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 318
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 264
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 72
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3464
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.252e1

DP
type: SiteQuality
SIO_000300: 1.92947e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.110000000000001e-2

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.827e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 2787
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 1.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 136
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 160
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 312
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1438
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.81e0

VQSLOD
type: SiteQuality
SIO_000300: 4.1e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.56e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

DP
type: SiteQuality
SIO_000300: 1.15983e5

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

GenotypeQuality
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bin: 2.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 604
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 82
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.516e1

VQSLOD
type: SiteQuality
SIO_000300: 1.97e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

DP
type: SiteQuality
SIO_000300: 6.3427e4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 9.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.021e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

GenotypeQuality
all individuals: 605
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.915708812260536e-3
allele num: 522
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 88
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.56e-1

DP
type: SiteQuality
SIO_000300: 4.3571e4

MQRankSum
type: SiteQuality
SIO_000300: -3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.019e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.56e-1

QD
type: SiteQuality
SIO_000300: 8.06e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -9.051e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.22e-1

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

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 114
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variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.162790697674419e-2
allele num: 86
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 504
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.36e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.09e-1

FS
type: SiteQuality
SIO_000300: 3.257e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.27e-1

QD
type: SiteQuality
SIO_000300: 1.502e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

DP
type: SiteQuality
SIO_000300: 4.0304e4

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

GenotypeQuality
all individuals: 37
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 93
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 86
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.984126984126984e-3
allele num: 504
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.36e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

QD
type: SiteQuality
SIO_000300: 1.502e1

FS
type: SiteQuality
SIO_000300: 3.257e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.09e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

DP
type: SiteQuality
SIO_000300: 4.0304e4

ClippingRankSum
type: SiteQuality
SIO_000300: -9.27e-1

GenotypeQuality
all individuals: 5
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 158
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variant carriers: 0

GenotypeQuality
all individuals: 9324
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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: 1
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GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 78
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.109704641350211e-3
allele num: 474
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.07e0

VQSLOD
type: SiteQuality
SIO_000300: -1.752e0

DP
type: SiteQuality
SIO_000300: 3.708e4

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.055e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.75e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.041e1

GenotypeQuality
all individuals: 50
bin: 3.25e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 39
bin: 3.75e1
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GenotypeQuality
all individuals: 200
bin: 1.75e1
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GenotypeQuality
all individuals: 213
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 70
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.380952380952381e-3
allele num: 420
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.38e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-1

QD
type: SiteQuality
SIO_000300: 1.29e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.67e-1

DP
type: SiteQuality
SIO_000300: 3.4385e4

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.18e-1

GenotypeQuality
all individuals: 1954
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 13

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1918
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variant carriers: 0

GenotypeQuality
all individuals: 2469
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.766472354707649e-4
allele num: 11322
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.436139656603051e-4
allele num: 62668
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.078981441519206e-4
allele num: 9268
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9336
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8360
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.288659793814433e-3
allele num: 776
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.75e0

VQSLOD
type: SiteQuality
SIO_000300: 4.41e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.024034e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.431e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.6e-2

GenotypeQuality
all individuals: 617
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
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GenotypeQuality
all individuals: 782
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4078
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9370
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.068832834544677e-4
allele num: 9356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62812
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8376
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11330
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 4.29e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.4e-1

FS
type: SiteQuality
SIO_000300: 2.307e0

MQRankSum
type: SiteQuality
SIO_000300: 4.53e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.173e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.81e0

DP
type: SiteQuality
SIO_000300: 2.0575e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.27e-1

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 2073
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GenotypeQuality
all individuals: 193
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GenotypeQuality
all individuals: 2017
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GenotypeQuality
all individuals: 484
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GenotypeQuality
all individuals: 10666
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GenotypeQuality
all individuals: 517
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GenotypeQuality
all individuals: 2636
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11350
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 782
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.125850340136054e-4
allele num: 9408
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63060
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9586
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.081521e6

VQSLOD
type: SiteQuality
SIO_000300: 2.82e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.05e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.100000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.349e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.53e-1

GenotypeQuality
all individuals: 20187
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 147
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1961
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2074
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3814
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9416
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.191327138432213e-4
allele num: 8394
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63106
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.169999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.287e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.62e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 6.99e-1

DP
type: SiteQuality
SIO_000300: 2.084713e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.96e0

MQ
type: SiteQuality
SIO_000300: 5.893e1

QD
type: SiteQuality
SIO_000300: 1.503e1

GenotypeQuality
all individuals: 90
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3818
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4188
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3102
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20194
bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63162
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9706
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11350
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9436
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.382086707956169e-4
allele num: 8396
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.16e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-1

DP
type: SiteQuality
SIO_000300: 2.08806e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.92e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.68e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

QD
type: SiteQuality
SIO_000300: 8.68e0

MQRankSum
type: SiteQuality
SIO_000300: -4.505e0

GenotypeQuality
all individuals: 183
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3818
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4983
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11025
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4188
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3102
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8396
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9436
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11350
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9706
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.749691270067446e-5
allele num: 63162
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.505e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.92e-1

DP
type: SiteQuality
SIO_000300: 2.08806e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.68e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.16e1

QD
type: SiteQuality
SIO_000300: 8.68e0

GenotypeQuality
all individuals: 458
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1891
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3107
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 188
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11139
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2076
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2660
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3395
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20191
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 1
allele frequency: 1.022285831118381e-4
allele num: 9782
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63228
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9456
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8396
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.888e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.97e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

DP
type: SiteQuality
SIO_000300: 2.090444e6

VQSLOD
type: SiteQuality
SIO_000300: -2.762e0

QD
type: SiteQuality
SIO_000300: 3.96e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e0

GenotypeQuality
all individuals: 103
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2703
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 543
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3118
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5094
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1616
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20209
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3850
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9516
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11386
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.575100806451613e-5
allele num: 63488
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8426
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10208
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.957e1

DP
type: SiteQuality
SIO_000300: 2.106481e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.79e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.34e-1

QD
type: SiteQuality
SIO_000300: 1.392e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.87e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

GenotypeQuality
all individuals: 3887
bin: 7.5e0
variant carriers: 563

GenotypeQuality
all individuals: 1390
bin: 7.25e1
variant carriers: 122

GenotypeQuality
all individuals: 863
bin: 9.25e1
variant carriers: 51

GenotypeQuality
all individuals: 2649
bin: 3.75e1
variant carriers: 368

GenotypeQuality
all individuals: 2804
bin: 3.25e1
variant carriers: 356

GenotypeQuality
all individuals: 1802
bin: 5.75e1
variant carriers: 189

GenotypeQuality
all individuals: 984
bin: 8.75e1
variant carriers: 62

GenotypeQuality
all individuals: 2116
bin: 6.25e1
variant carriers: 156

GenotypeQuality
all individuals: 2436
bin: 4.25e1
variant carriers: 314

GenotypeQuality
all individuals: 1264
bin: 7.75e1
variant carriers: 115

African
type: Population
allele count: 316
allele frequency: 4.977945809703844e-2
allele num: 6348
num of homozygotes: 0

South Asian
type: Population
allele count: 589
allele frequency: 8.139856274184633e-2
allele num: 7236
num of homozygotes: 0

Latino
type: Population
allele count: 423
allele frequency: 5.244235060748823e-2
allele num: 8066
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 66
allele frequency: 1.614481409001957e-2
allele num: 4088
num of homozygotes: 0

Other
type: Population
allele count: 18
allele frequency: 3.249097472924187e-2
allele num: 554
num of homozygotes: 0

East Asian
type: Population
allele count: 325
allele frequency: 5.83902263744161e-2
allele num: 5566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1674
allele frequency: 3.927364864864865e-2
allele num: 42624
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.62e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.26e-1

QD
type: SiteQuality
SIO_000300: 1.36e0

DP
type: SiteQuality
SIO_000300: 3.070987e6

MQ
type: SiteQuality
SIO_000300: 5.936e1

VQSLOD
type: SiteQuality
SIO_000300: 2.51e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.0e-3

FS
type: SiteQuality
SIO_000300: 9.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.28e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.02e-1

GenotypeQuality
all individuals: 3887
bin: 7.5e0
variant carriers: 5

GenotypeQuality
all individuals: 3018
bin: 2.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1264
bin: 7.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3529
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 863
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2436
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1390
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 984
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1802
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1639
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6348
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.876876876876877e-4
allele num: 42624
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.593244699964068e-4
allele num: 5566
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4088
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.239771881973717e-4
allele num: 8066
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 554
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 9.673852957435047e-4
allele num: 7236
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.36e0

FS
type: SiteQuality
SIO_000300: 9.59e-1

DP
type: SiteQuality
SIO_000300: 3.070987e6

MQ
type: SiteQuality
SIO_000300: 5.936e1

VQSLOD
type: SiteQuality
SIO_000300: 2.51e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.62e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.26e-1

GenotypeQuality
all individuals: 3116
bin: 1.75e1
variant carriers: 1063

GenotypeQuality
all individuals: 3887
bin: 7.5e0
variant carriers: 1251

GenotypeQuality
all individuals: 2027
bin: 5.25e1
variant carriers: 1031

GenotypeQuality
all individuals: 1132
bin: 8.25e1
variant carriers: 618

GenotypeQuality
all individuals: 2804
bin: 3.25e1
variant carriers: 1083

GenotypeQuality
all individuals: 8211
bin: 9.75e1
variant carriers: 6110

GenotypeQuality
all individuals: 1639
bin: 6.75e1
variant carriers: 797

GenotypeQuality
all individuals: 1802
bin: 5.75e1
variant carriers: 896

GenotypeQuality
all individuals: 863
bin: 9.25e1
variant carriers: 513

GenotypeQuality
all individuals: 2116
bin: 6.25e1
variant carriers: 886

Latino
type: Population
allele count: 2442
allele frequency: 3.027522935779817e-1
allele num: 8066
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 353
allele frequency: 8.635029354207437e-2
allele num: 4088
num of homozygotes: 0

African
type: Population
allele count: 1423
allele frequency: 2.241650913673598e-1
allele num: 6348
num of homozygotes: 0

East Asian
type: Population
allele count: 1297
allele frequency: 2.330219187926698e-1
allele num: 5566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11167
allele frequency: 2.619885510510511e-1
allele num: 42624
num of homozygotes: 0

Other
type: Population
allele count: 141
allele frequency: 2.545126353790614e-1
allele num: 554
num of homozygotes: 0

South Asian
type: Population
allele count: 2295
allele frequency: 3.171641791044776e-1
allele num: 7236
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.936e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.51e0

QD
type: SiteQuality
SIO_000300: 1.36e0

FS
type: SiteQuality
SIO_000300: 9.59e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.26e-1

DP
type: SiteQuality
SIO_000300: 3.070987e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.62e-2

GenotypeQuality
all individuals: 984
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3887
bin: 7.5e0
variant carriers: 28

GenotypeQuality
all individuals: 1639
bin: 6.75e1
variant carriers: 7

GenotypeQuality
all individuals: 11883
bin: 2.5e0
variant carriers: 34

GenotypeQuality
all individuals: 1390
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 1132
bin: 8.25e1
variant carriers: 6

GenotypeQuality
all individuals: 1264
bin: 7.75e1
variant carriers: 7

GenotypeQuality
all individuals: 1802
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 8211
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 2436
bin: 4.25e1
variant carriers: 8

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4088
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 3.719315645921151e-4
allele num: 8066
num of homozygotes: 0

South Asian
type: Population
allele count: 15
allele frequency: 2.072968490878939e-3
allele num: 7236
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 1.07797340998922e-3
allele num: 5566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 61
allele frequency: 1.431118618618619e-3
allele num: 42624
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 5.415162454873646e-3
allele num: 554
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 1.102709514807813e-3
allele num: 6348
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.28e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.51e0

MQRankSum
type: SiteQuality
SIO_000300: 2.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.62e-2

DP
type: SiteQuality
SIO_000300: 3.070987e6

QD
type: SiteQuality
SIO_000300: 1.36e0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5566
num of homozygotes: 0

African
type: Population
allele count: 197
allele frequency: 3.103339634530561e-2
allele num: 6348
num of homozygotes: 4

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.173048048048048e-4
allele num: 42624
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.36e0

FS
type: SiteQuality
SIO_000300: 9.59e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.62e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.28e-1

DP
type: SiteQuality
SIO_000300: 3.070987e6

VQSLOD
type: SiteQuality
SIO_000300: 2.51e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.26e-1

GenotypeQuality
all individuals: 140
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 676
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variant carriers: 0

GenotypeQuality
all individuals: 3487
bin: 6.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
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: 9906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65108
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13016
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.695652173913044e-5
allele num: 11500
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.11e0

VQSLOD
type: SiteQuality
SIO_000300: 1.77e-1

QD
type: SiteQuality
SIO_000300: 1.239e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.287e0

DP
type: SiteQuality
SIO_000300: 3.112629e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

MQRankSum
type: SiteQuality
SIO_000300: -6.929999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.96e-1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2774
bin: 8.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9942
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.612667478684531e-5
allele num: 13136
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65122
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.69e0

FS
type: SiteQuality
SIO_000300: 1.04e1

MQ
type: SiteQuality
SIO_000300: 5.899e1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.92e0

QD
type: SiteQuality
SIO_000300: 1.098e1

VQSLOD
type: SiteQuality
SIO_000300: -4.078e0

DP
type: SiteQuality
SIO_000300: 3.114872e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e0

GenotypeQuality
all individuals: 718
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3005
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variant carriers: 0

GenotypeQuality
all individuals: 2648
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.150250622712876e-5
allele num: 65038
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12638
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9978
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.122e0

MQ
type: SiteQuality
SIO_000300: 5.949e1

FS
type: SiteQuality
SIO_000300: 1.991e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

QD
type: SiteQuality
SIO_000300: 2.46e0

MQRankSum
type: SiteQuality
SIO_000300: 1.57e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.8e-2

DP
type: SiteQuality
SIO_000300: 3.122356e6

GenotypeQuality
all individuals: 75
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2013
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2841
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 3.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14246
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517358582180141e-5
allele num: 65904
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-1

DP
type: SiteQuality
SIO_000300: 3.154067e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.088e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.97e-1

FS
type: SiteQuality
SIO_000300: 1.026e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.83e-1

QD
type: SiteQuality
SIO_000300: 1.163e1

GenotypeQuality
all individuals: 6197
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3043
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 50
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GenotypeQuality
all individuals: 3174
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66008
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14584
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.070000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.28e-1

DP
type: SiteQuality
SIO_000300: 3.16187e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.842e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

MQ
type: SiteQuality
SIO_000300: 5.835e1

VQSLOD
type: SiteQuality
SIO_000300: -1.283e0

QD
type: SiteQuality
SIO_000300: 2.164e1

GenotypeQuality
all individuals: 295
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2106
bin: 8.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447535e-5
allele num: 66140
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14882
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.597e0

MQRankSum
type: SiteQuality
SIO_000300: 6.62e-1

MQ
type: SiteQuality
SIO_000300: 5.909e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.9e-2

QD
type: SiteQuality
SIO_000300: 1.275e1

DP
type: SiteQuality
SIO_000300: 3.170266e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.05e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.345e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.0e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15384
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66302
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -8.47e-1

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -7.35e-1

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.47e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.315e0

MQ
type: SiteQuality
SIO_000300: 5.885e1

DP
type: SiteQuality
SIO_000300: 3.180449e6

GenotypeQuality
all individuals: 118
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15602
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505661286437003e-5
allele num: 66416
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.33e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.032e-1

DP
type: SiteQuality
SIO_000300: 3.185349e6

MQRankSum
type: SiteQuality
SIO_000300: -2.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

MQ
type: SiteQuality
SIO_000300: 5.984e1

FS
type: SiteQuality
SIO_000300: 3.564e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.33e-1

QD
type: SiteQuality
SIO_000300: 1.793e1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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: 49
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GenotypeQuality
all individuals: 35273
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
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: 10394
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.324310650139134e-5
allele num: 15812
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66464
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.01e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e-1

FS
type: SiteQuality
SIO_000300: 5.83e0

MQRankSum
type: SiteQuality
SIO_000300: 7.56e-1

QD
type: SiteQuality
SIO_000300: 1.148e1

DP
type: SiteQuality
SIO_000300: 3.18982e6

MQ
type: SiteQuality
SIO_000300: 6.022e1

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 13

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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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: 53
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.202826642610134e-4
allele num: 66510
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.885725278953444e-4
allele num: 10396
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15940
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.200000000000001e-3

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -2.4e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.193617e6

MQRankSum
type: SiteQuality
SIO_000300: 4.07e-1

MQ
type: SiteQuality
SIO_000300: 5.941e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.34e-1

QD
type: SiteQuality
SIO_000300: 1.07e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.392e0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2128
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66556
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: 16090
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.311604253351826e-4
allele num: 8652
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.64e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.81e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.57e-1

QD
type: SiteQuality
SIO_000300: 1.126e1

FS
type: SiteQuality
SIO_000300: 6.212e0

VQSLOD
type: SiteQuality
SIO_000300: 4.29e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

DP
type: SiteQuality
SIO_000300: 3.19589e6

GenotypeQuality
all individuals: 194
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variant carriers: 0

GenotypeQuality
all individuals: 25
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2928
bin: 7.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 16
allele frequency: 1.849283402681461e-3
allele num: 8652
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.923076923076923e-4
allele num: 10400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501276084671971e-5
allele num: 66610
num of homozygotes: 0

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

South Asian
type: Population
allele count: 10
allele frequency: 6.146281499692685e-4
allele num: 16270
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e-1

DP
type: SiteQuality
SIO_000300: 3.201487e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.188e0

MQRankSum
type: SiteQuality
SIO_000300: 1.2e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

VQSLOD
type: SiteQuality
SIO_000300: 4.8e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.274e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 5
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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
all individuals: 2882
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GenotypeQuality
all individuals: 91
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variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16420
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: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.41e-1

FS
type: SiteQuality
SIO_000300: 5.663e0

MQRankSum
type: SiteQuality
SIO_000300: -2.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.21e0

DP
type: SiteQuality
SIO_000300: 3.201196e6

MQ
type: SiteQuality
SIO_000300: 5.979e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.54e-1

QD
type: SiteQuality
SIO_000300: 1.378e1

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3060
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16450
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: 11576
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66666
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.201624e6

FS
type: SiteQuality
SIO_000300: 5.192e0

QD
type: SiteQuality
SIO_000300: 1.178e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.738e0

MQRankSum
type: SiteQuality
SIO_000300: 6.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.359e0

MQ
type: SiteQuality
SIO_000300: 5.842e1

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3061
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 35277
bin: 9.75e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.499235130027895e-5
allele num: 66678
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
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: 10404
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.202539e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.34e0

MQ
type: SiteQuality
SIO_000300: 5.934e1

VQSLOD
type: SiteQuality
SIO_000300: 1.53e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.95e-1

FS
type: SiteQuality
SIO_000300: 1.805e0

MQRankSum
type: SiteQuality
SIO_000300: -4.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.153e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.95e-1

GenotypeQuality
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variant carriers: 4

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

African
type: Population
allele count: 16
allele frequency: 1.540832049306626e-3
allele num: 10384
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 97
allele frequency: 1.45860274878951e-3
allele num: 66502
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 7
allele frequency: 6.051175656984786e-4
allele num: 11568
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.14e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.06e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

MQRankSum
type: SiteQuality
SIO_000300: 6.53e-1

QD
type: SiteQuality
SIO_000300: 5.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.31e0

DP
type: SiteQuality
SIO_000300: 3.229385e6

GenotypeQuality
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variant carriers: 16

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3609
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variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
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: 15
allele frequency: 9.092011152867014e-4
allele num: 16498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66702
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.927e1

MQRankSum
type: SiteQuality
SIO_000300: 2.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.43e-1

DP
type: SiteQuality
SIO_000300: 3.216008e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -7.206e-1

FS
type: SiteQuality
SIO_000300: 9.414999999999999e0

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -5.85e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.46e-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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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.728011059270779e-4
allele num: 11574
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.922337562475971e-4
allele num: 10404
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
num of homozygotes: 0

Other
type: Population
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East Asian
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allele frequency: 0.0e0
allele num: 8654
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MQ
type: SiteQuality
SIO_000300: 5.927e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.43e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 9.414999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.85e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.66e-1

InbreedingCoeff
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DP
type: SiteQuality
SIO_000300: 3.216008e6

QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2883
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variant carriers: 0

Latino
type: Population
allele count: 0
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allele num: 11572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998500749625187e-5
allele num: 66700
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 4.09e-1

FS
type: SiteQuality
SIO_000300: 1.819e0

QD
type: SiteQuality
SIO_000300: 1.175e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.447e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

DP
type: SiteQuality
SIO_000300: 3.21545e6

GenotypeQuality
all individuals: 2935
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35336
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 35
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 3610
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2883
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8535
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3055
bin: 9.25e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66700
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.0e-2

FS
type: SiteQuality
SIO_000300: 1.819e0

QD
type: SiteQuality
SIO_000300: 1.175e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.79e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.09e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.447e0

DP
type: SiteQuality
SIO_000300: 3.21545e6

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

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

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

GenotypeQuality
all individuals: 8527
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2935
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2882
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 5.75e1
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: 11568
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.945e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 3.215381e6

QD
type: SiteQuality
SIO_000300: 2.05e0

MQRankSum
type: SiteQuality
SIO_000300: -1.3e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.193e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.646e0

FS
type: SiteQuality
SIO_000300: 8.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.92e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0