3-133560100-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560100
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560100
    reference: chr 3
allele count: 6
allele frequency: 4.981816370248592e-5
allele num: 120438
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.190+29G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13271G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.289+29G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.289+29G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.127+29G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.250+29G>A
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10252
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19973
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17802
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30779
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1042
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 670
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2311
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9968
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3727
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/3-133560102-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560102
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560102
    reference: chr 3
allele count: 1
allele frequency: 8.299581701082266e-6
allele num: 120488
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13273G>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.127+27G>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.289+27G>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.289+27G>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.190+27G>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.250+27G>T
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10346
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20202
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4065
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17897
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 550
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31163
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2303
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 1045
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3741
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4323
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ

3-133560103-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560103
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560102
    reference: chr 3
allele count: 1
allele frequency: 8.2936619835122e-6
allele num: 120574
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.250+25delG
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.289+25delG
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.190+25delG
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.127+25delG
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.289+25delG
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13275delG
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4062
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17998
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20286
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 3753
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 31470
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genotype quality: GenotypeQuality
  all individuals: 4326
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 191
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genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: TC
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

3-133560110-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560110
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560110
    reference: chr 3
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.289+19C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13281C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.190+19C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.127+19C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.289+19C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.250+19C>T
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20714
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10429
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
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genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4072
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  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18503
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3772
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3468
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32630
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2296
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4325
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 131
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: QD

3-133560111-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560111
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560111
    reference: chr 3
allele count: 6
allele frequency: 4.967380865648906e-5
allele num: 120788
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.190+18C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13282C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.127+18C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.289+18C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.250+18C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.289+18C>T
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4075
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20759
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1253
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32722
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1046
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2295
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3473
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10184
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

3-133560130-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560130
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560130
    reference: chr 3
allele count: 1
allele frequency: 8.255865792645674e-6
allele num: 121126
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13301A>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.249A>C
  hgvsp: ENST00000486858.1:c.249A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.288A>C
  hgvsp: ENST00000543906.1:c.288A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.189A>C
  hgvsp: ENST00000477759.1:c.189A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.126A>C
  hgvsp: ENST00000460865.3:c.126A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.288A>C
  hgvsp: ENST00000285208.4:c.288A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4075
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10551
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21251
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33617
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1254
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1049
  bin: 8.75e1
  variant carriers: 0
hgvs: c.288A>C
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum

3-133560136-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560136
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560136
    reference: chr 3
allele count: 4
allele frequency: 3.301092661671013e-5
allele num: 121172
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.183C>T
  hgvsp: ENST00000477759.1:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.120C>T
  hgvsp: ENST00000460865.3:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.282C>T
  hgvsp: ENST00000543906.1:c.282C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.282C>T
  hgvsp: ENST00000285208.4:c.282C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.243C>T
  hgvsp: ENST00000486858.1:c.243C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13307C>T
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18771
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10553
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21298
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4325
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1047
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3489
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp94Asp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

3-133560138-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560138
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560138
    reference: chr 3
allele count: 4
allele frequency: 3.300983693140556e-5
allele num: 121176
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.241G>A
  hgvsp: ENSP00000419381.1:p.Asp81Asn
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.118G>A
  hgvsp: ENSP00000419526.3:p.Asp40Asn
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.280G>A
  hgvsp: ENSP00000437797.1:p.Asp94Asn
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.181G>A
  hgvsp: ENSP00000419941.1:p.Asp61Asn
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.280G>A
  hgvsp: ENSP00000285208.4:p.Asp94Asn
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13309G>A
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10562
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18757
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21313
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3487
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4325
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2304
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33699
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asp94Asn
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

3-133560139-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560139
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560139
    reference: chr 3
allele count: 15
allele frequency: 1.237807595187404e-4
allele num: 121182
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.117C>T
  hgvsp: ENST00000460865.3:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.180C>T
  hgvsp: ENST00000477759.1:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.279C>T
  hgvsp: ENST00000285208.4:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13310C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.240C>T
  hgvsp: ENST00000486858.1:c.240C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.279C>T
  hgvsp: ENST00000543906.1:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18740
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10576
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 21318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3797
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1255
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1048
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Tyr93Tyr
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

3-133560142-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560142
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560142
    reference: chr 3
allele count: 1
allele frequency: 8.250144377526608e-6
allele num: 121210
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13313G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.276G>A
  hgvsp: ENST00000285208.4:c.276G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.177G>A
  hgvsp: ENST00000477759.1:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.276G>A
  hgvsp: ENST00000543906.1:c.276G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.114G>A
  hgvsp: ENST00000460865.3:c.114G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.237G>A
  hgvsp: ENST00000486858.1:c.237G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18739
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10572
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21355
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4081
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1257
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10330
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2304
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1048
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4321
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Val92Val
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

3-133560157-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560157
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560157
    reference: chr 3
allele count: 9
allele frequency: 7.422802850356295e-5
allele num: 121248
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13328G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.162G>A
  hgvsp: ENST00000477759.1:c.162G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.99G>A
  hgvsp: ENST00000460865.3:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.261G>A
  hgvsp: ENST00000285208.4:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.261G>A
  hgvsp: ENST00000543906.1:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.222G>A
  hgvsp: ENST00000486858.1:c.222G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10592
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18716
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21412
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1049
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2307
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33760
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr87Thr
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

3-133560172-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560172
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560172
    reference: chr 3
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.147C>T
  hgvsp: ENST00000477759.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.84C>T
  hgvsp: ENST00000460865.3:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.246C>T
  hgvsp: ENST00000285208.4:c.246C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.246C>T
  hgvsp: ENST00000543906.1:c.246C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13343C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.207C>T
  hgvsp: ENST00000486858.1:c.207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.147C>T
  hgvsp: ENST00000488969.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18716
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10599
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4324
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33860
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Tyr82Tyr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

3-133560181-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560181
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560181
    reference: chr 3
allele count: 1
allele frequency: 8.244702778464837e-6
allele num: 121290
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.237C>A
  hgvsp: ENST00000285208.4:c.237C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.138C>A
  hgvsp: ENST00000477759.1:c.138C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.237C>A
  hgvsp: ENST00000543906.1:c.237C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.75C>A
  hgvsp: ENST00000460865.3:c.75C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.138C>A
  hgvsp: ENST00000488969.1:c.138C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13352C>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.198C>A
  hgvsp: ENST00000486858.1:c.198C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21480
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10597
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18677
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2302
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3494
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1252
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile79Ile
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

3-133560191-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560191
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560191
    reference: chr 3
allele count: 1
allele frequency: 8.245110649384915e-6
allele num: 121284
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.65G>A
  hgvsp: ENSP00000419526.3:p.Arg22His
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13362G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.128G>A
  hgvsp: ENSP00000419941.1:p.Arg43His
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.227G>A
  hgvsp: ENSP00000285208.4:p.Arg76His
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.188G>A
  hgvsp: ENSP00000419381.1:p.Arg63His
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.128G>A
  hgvsp: ENSP00000417433.1:p.Arg43His
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.227G>A
  hgvsp: ENSP00000437797.1:p.Arg76His
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18668
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21475
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10600
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4322
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1048
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10319
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1252
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33823
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg76His
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

3-133560196-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560196
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560196
    reference: chr 3
allele count: 2
allele frequency: 1.649049323065253e-5
allele num: 121282
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.222G>A
  hgvsp: ENST00000543906.1:c.222G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13367G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.183G>A
  hgvsp: ENST00000486858.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.60G>A
  hgvsp: ENST00000460865.3:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.222G>A
  hgvsp: ENST00000285208.4:c.222G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.123G>A
  hgvsp: ENST00000477759.1:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.123G>A
  hgvsp: ENST00000488969.1:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18647
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10595
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3487
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3793
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg74Arg
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

3-133560205-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560205
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560205
    reference: chr 3
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.114T>C
  hgvsp: ENST00000477759.1:c.114T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13376T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.174T>C
  hgvsp: ENST00000486858.1:c.174T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.114T>C
  hgvsp: ENST00000488969.1:c.114T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.213T>C
  hgvsp: ENST00000543906.1:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.51T>C
  hgvsp: ENST00000460865.3:c.51T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.213T>C
  hgvsp: ENST00000285208.4:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18632
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4079
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3789
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3488
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly71Gly
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum

3-133560208-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560208
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560208
    reference: chr 3
allele count: 1
allele frequency: 8.246878556466378e-6
allele num: 121258
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.111T>C
  hgvsp: ENST00000477759.1:c.111T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.171T>C
  hgvsp: ENST00000486858.1:c.171T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.210T>C
  hgvsp: ENST00000285208.4:c.210T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.210T>C
  hgvsp: ENST00000543906.1:c.210T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13379T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.111T>C
  hgvsp: ENST00000488969.1:c.111T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.48T>C
  hgvsp: ENST00000460865.3:c.48T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18627
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10593
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1048
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2298
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3793
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3483
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1252
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala70Ala
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

3-133560232-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560232
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560232
    reference: chr 3
allele count: 2
allele frequency: 1.650791554550407e-5
allele num: 121154
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.186G>A
  hgvsp: ENST00000285208.4:c.186G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.186G>A
  hgvsp: ENST00000543906.1:c.186G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.147G>A
  hgvsp: ENST00000486858.1:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.24G>A
  hgvsp: ENST00000460865.3:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.87G>A
  hgvsp: ENST00000488969.1:c.87G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.87G>A
  hgvsp: ENST00000477759.1:c.87G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13403G>A
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18316
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10574
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3471
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33445
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10272
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4321
  bin: 9.75e1
  variant carriers: 2
hgvs: c.186G>A
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

3-133560234-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560234
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560234
    reference: chr 3
allele count: 1
allele frequency: 8.254094030639197e-6
allele num: 121152
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.22G>A
  hgvsp: ENSP00000419526.3:p.Val8Met
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.184G>A
  hgvsp: ENSP00000437797.1:p.Val62Met
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.85G>A
  hgvsp: ENSP00000419941.1:p.Val29Met
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13405G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.145G>A
  hgvsp: ENSP00000419381.1:p.Val49Met
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.184G>A
  hgvsp: ENSP00000285208.4:p.Val62Met
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.85G>A
  hgvsp: ENSP00000417433.1:p.Val29Met
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10575
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18276
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4079
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3766
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2297
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val62Met
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD

3-133560237-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560237
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560237
    reference: chr 3
allele count: 1
allele frequency: 8.257092842751923e-6
allele num: 121108
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.22-3C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.85-3C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13408C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.184-3C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.85-3C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.145-3C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.184-3C>T
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21503
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18088
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10572
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33178
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3468
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: c.184-3C>T
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD

3-133560247-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560247
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560247
    reference: chr 3
allele count: 7
allele frequency: 5.787228413638017e-5
allele num: 120956
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.145-13C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.184-13C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13418C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.22-13C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.85-13C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.184-13C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.85-13C>T
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17574
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4071
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21341
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10524
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32571
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4323
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD

3-133560248-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560248
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560248
    reference: chr 3
allele count: 1
allele frequency: 8.268289456277286e-6
allele num: 120944
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.184-14C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.22-14C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.85-14C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.85-14C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.145-14C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13419C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.184-14C>T
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4072
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10524
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17502
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21305
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2296
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10113
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  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: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

3-133560252-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560252
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560252
    reference: chr 3
allele count: 1
allele frequency: 8.27348843366317e-6
allele num: 120868
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.184-18C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.145-18C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.85-18C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.22-18C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.85-18C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13423C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.184-18C>T
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4081
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10494
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16841
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21089
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3407
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31539
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4315
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ

3-133560258-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560258
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560258
    reference: chr 3
allele count: 6
allele frequency: 4.968368056705641e-5
allele num: 120764
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.85-24A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.145-24A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13429A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.184-24A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.85-24A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.22-24A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.184-24A>G
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4068
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20580
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15781
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4318
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1043
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29915
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1401
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3694
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3378
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9877
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD

3-133560265-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560265
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560265
    reference: chr 3
allele count: 1
allele frequency: 8.29132395860971e-6
allele num: 120608
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.85-31T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.184-31T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13436T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.85-31T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.145-31T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.184-31T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.22-31T>C
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2694
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10040
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1033
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3271
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1243
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1967
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3610
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

3-133560267-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560267
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560267
    reference: chr 3
allele count: 1
allele frequency: 8.298066550493736e-6
allele num: 120510
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.184-33C>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.85-33C>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13438C>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.145-33C>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.22-33C>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.85-33C>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.184-33C>G
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5717
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18669
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13608
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9835
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2868
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4025
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2209
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2044
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1031
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 933
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24772
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1320
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3572
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2307
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD

3-133560269-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560269
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560269
    reference: chr 3
allele count: 1
allele frequency: 8.298341991270144e-6
allele num: 120506
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13440C>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.85-35C>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.85-35C>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.22-35C>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.184-35C>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.145-35C>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.184-35C>A
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18683
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4017
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5707
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9741
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 938
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2239
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8928
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2045
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 772
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2303
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

3-133560273-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560273
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560273
    reference: chr 3
allele count: 1
allele frequency: 8.30813199960121e-6
allele num: 120364
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.145-39C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.85-39C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13444C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.184-39C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.22-39C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.85-39C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.184-39C>T
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13403
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9325
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7860
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2942
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3093
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2950
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8308
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3492
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1510
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1594
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1237
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

3-133560274-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560274
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560274
    reference: chr 3
allele count: 1
allele frequency: 8.3099270388406e-6
allele num: 120338
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.22-40A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.85-40A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.184-40A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.145-40A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.85-40A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13445A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.184-40A>G
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1949
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9297
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13435
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7850
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3974
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2949
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17167
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4309
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3081
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1589
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3480
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1273
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1237
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22793
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2960
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

3-133560274-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560274
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560275
    reference: chr 3
allele count: 1
allele frequency: 8.3099270388406e-6
allele num: 120338
alternate allele: TG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.85-41dupC
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.184-41dupC
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13446dupC
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.145-41dupC
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.85-41dupC
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.184-41dupC
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.22-41dupC
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3974
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17167
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2949
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13435
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9297
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7850
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1949
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3046
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2218
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1520
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1026
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3081
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22793
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8296
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2960
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP

3-133560279-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560279
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560279
    reference: chr 3
allele count: 14
allele frequency: 1.166900046676002e-4
allele num: 119976
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.184-45G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.145-45G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.85-45G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.85-45G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.22-45G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13450G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.184-45G>A
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15435
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8246
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8818
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3950
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1229
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2963
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1730
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7795
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3396
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2480
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3950
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3603
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/3-133560280-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560280
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560280
    reference: chr 3
allele count: 1
allele frequency: 8.326256015719971e-6
allele num: 120102
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.85-46T>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.22-46T>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13451T>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.145-46T>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.85-46T>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.184-46T>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.184-46T>G
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15244
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8747
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2976
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3406
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4303
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1231
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1021
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2495
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

3-133560283-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560283
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560283
    reference: chr 3
allele count: 15
allele frequency: 1.251355635271544e-4
allele num: 119870
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.184-49C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.85-49C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.85-49C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.22-49C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.145-49C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.184-49C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13454C>T
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3939
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15792
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8670
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8166
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2952
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15034
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4315
  bin: 9.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 2941
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3531
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4353
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3381
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1330
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 1
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

3-133560404-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560404
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560404
    reference: chr 3
allele count: 7
allele frequency: 5.876525797948253e-5
allele num: 119118
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.183+50C>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.84+50C>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.144+50C>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.21+50C>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13575C>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.84+50C>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.183+50C>A
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2571
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10817
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8994
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4304
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2887
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22372
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 924
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4355
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4563
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2403
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1018
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 671
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ

http://identifiers.org/exac.variant/3-133560405-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560405
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560405
    reference: chr 3
allele count: 1
allele frequency: 8.398280032249395e-6
allele num: 119072
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13576G>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.183+49G>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.84+49G>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.21+49G>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.144+49G>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.84+49G>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.183+49G>T
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9266
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2512
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8991
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4334
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6911
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1004
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 958
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 976
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 912
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 989
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22373
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4341
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

3-133560405-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560405
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560405
    reference: chr 3
allele count: 1
allele frequency: 8.398280032249395e-6
allele num: 119072
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.144+49G>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.84+49G>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13576G>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.21+49G>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.183+49G>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.84+49G>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.183+49G>C
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6911
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2512
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4334
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8991
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10830
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9266
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5331
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 912
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1004
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 976
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 958
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2396
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22373
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP

3-133560405-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560405
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560405
    reference: chr 3
allele count: 15
allele frequency: 1.259742004837409e-4
allele num: 119072
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.84+49G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.144+49G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.21+49G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13576G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.183+49G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.183+49G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.84+49G>A
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2512
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10830
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9266
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8991
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4334
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6911
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 989
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 912
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3596
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 976
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4575
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4341
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum

3-133560411-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560411
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560411
    reference: chr 3
allele count: 1
allele frequency: 8.383775717232013e-6
allele num: 119278
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.84+43C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.183+43C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13582C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.84+43C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.144+43C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.21+43C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.183+43C>T
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9008
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4944
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4632
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10979
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2924
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 919
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1070
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3601
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5428
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: African
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

3-133560413-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560413
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560413
    reference: chr 3
allele count: 2
allele frequency: 1.675462846611376e-5
allele num: 119370
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.84+41T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13584T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.183+41T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.144+41T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.183+41T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.21+41T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.84+41T>C
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5082
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4640
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9008
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6915
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 892
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2927
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1091
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3605
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

3-133560414-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560414
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560414
    reference: chr 3
allele count: 1
allele frequency: 8.377314233056882e-6
allele num: 119370
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.183+40T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.84+40T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.183+40T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.21+40T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.144+40T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13585T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.84+40T>C
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5099
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11016
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9016
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6919
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4632
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 873
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5439
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9924
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2387
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2922
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4576
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ

3-133560423-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560423
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560423
    reference: chr 3
allele count: 8987
allele frequency: 7.498790113979607e-2
allele num: 119846
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.84+31C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13594C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.21+31C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.183+31C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.144+31C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.183+31C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.84+31C>T
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6553
  bin: 4.25e1
  variant carriers: 770
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 6.75e1
  variant carriers: 605
genotype depth: GenotypeDepth
  all individuals: 10379
  bin: 3.25e1
  variant carriers: 438
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 9.75e1
  variant carriers: 753
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 7.5e0
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 5.75e1
  variant carriers: 884
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 7.25e1
  variant carriers: 421
genotype depth: GenotypeDepth
  all individuals: 8385
  bin: 3.75e1
  variant carriers: 619
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4684
  bin: 4.75e1
  variant carriers: 963
genotype depth: GenotypeDepth
  all individuals: 9353
  bin: 2.75e1
  variant carriers: 282
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 8.75e1
  variant carriers: 162
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 1.75e1
  variant carriers: 139
genotype depth: GenotypeDepth
  all individuals: 5278
  bin: 2.25e1
  variant carriers: 164
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 8.25e1
  variant carriers: 204
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.75e1
  variant carriers: 284
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 1.25e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.25e1
  variant carriers: 121
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 6.25e1
  variant carriers: 719
genotype depth: GenotypeDepth
  all individuals: 3233
  bin: 5.25e1
  variant carriers: 960
genotype quality: GenotypeQuality
  all individuals: 584
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10645
  bin: 6.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3076
  bin: 9.25e1
  variant carriers: 14
num of homozygotes: 432
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

3-133560428-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560428
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560428
    reference: chr 3
allele count: 9
allele frequency: 7.499750008333055e-5
allele num: 120004
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.21+26A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.183+26A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13599A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.84+26A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.144+26A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.183+26A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.84+26A>G
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10570
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6857
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5790
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4521
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9054
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3062
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6041
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21032
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4502
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

3-133560431-CAGT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560431
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560428
    reference: chr 3
allele count: 2
allele frequency: 1.664918502239315e-5
allele num: 120126
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.144+20_144+22delACT
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.84+20_84+22delACT
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.21+20_21+22delACT
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.84+20_84+22delACT
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.183+20_183+22delACT
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.183+20_183+22delACT
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13605_96-13603delACT
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4517
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9059
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10680
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11533
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6854
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3059
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3653
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 740
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: CAGT
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

3-133560454-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560454
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560454
    reference: chr 3
allele count: 3
allele frequency: 2.483484825907714e-5
allele num: 120798
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.84G>A
  hgvsp: ENST00000477759.1:c.84G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.183G>A
  hgvsp: ENST00000543906.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.84G>A
  hgvsp: ENST00000488969.1:c.84G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13625G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.183G>A
  hgvsp: ENST00000285208.4:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.21G>A
  hgvsp: ENST00000460865.3:c.21G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.144G>A
  hgvsp: ENST00000486858.1:c.144G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9052
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11152
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6998
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11586
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14500
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21061
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: c.183G>A
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: C
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS

3-133560455-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560455
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560455
    reference: chr 3
allele count: 2
allele frequency: 1.655108492361674e-5
allele num: 120838
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.182C>T
  hgvsp: ENSP00000437797.1:p.Thr61Met
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.83C>T
  hgvsp: ENSP00000419941.1:p.Thr28Met
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.83C>T
  hgvsp: ENSP00000417433.1:p.Thr28Met
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.182C>T
  hgvsp: ENSP00000285208.4:p.Thr61Met
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13626C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.143C>T
  hgvsp: ENSP00000419381.1:p.Thr48Met
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.20C>T
  hgvsp: ENSP00000419526.3:p.Thr7Met
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11172
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1894
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7018
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9054
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6846
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11589
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr61Met
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

3-133560458-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560458
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560458
    reference: chr 3
allele count: 1
allele frequency: 8.272119647938589e-6
allele num: 120888
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.179G>A
  hgvsp: ENSP00000285208.4:p.Arg60His
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.80G>A
  hgvsp: ENSP00000419941.1:p.Arg27His
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.179G>A
  hgvsp: ENSP00000437797.1:p.Arg60His
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.17G>A
  hgvsp: ENSP00000419526.3:p.Arg6His
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.80G>A
  hgvsp: ENSP00000417433.1:p.Arg27His
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13629G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.140G>A
  hgvsp: ENSP00000419381.1:p.Arg47His
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11610
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6847
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4517
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9060
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1894
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4503
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3650
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3076
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg60His
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

3-133560462-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560462
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560462
    reference: chr 3
allele count: 1
allele frequency: 8.26801600687899e-6
allele num: 120948
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.175G>A
  hgvsp: ENSP00000437797.1:p.Asp59Asn
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.136G>A
  hgvsp: ENSP00000419381.1:p.Asp46Asn
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.76G>A
  hgvsp: ENSP00000417433.1:p.Asp26Asn
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.76G>A
  hgvsp: ENSP00000419941.1:p.Asp26Asn
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.13G>A
  hgvsp: ENSP00000419526.3:p.Asp5Asn
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13633G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.175G>A
  hgvsp: ENSP00000285208.4:p.Asp59Asn
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7011
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11292
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9047
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6841
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6220
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asp59Asn
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum

3-133560468-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560468
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560468
    reference: chr 3
allele count: 2
allele frequency: 1.652892561983471e-5
allele num: 121000
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13639T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.70T>C
  hgvsp: ENST00000488969.1:c.70T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.130T>C
  hgvsp: ENST00000486858.1:c.130T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.169T>C
  hgvsp: ENST00000285208.4:c.169T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.169T>C
  hgvsp: ENST00000543906.1:c.169T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.70T>C
  hgvsp: ENST00000477759.1:c.70T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.7T>C
  hgvsp: ENST00000460865.3:c.7T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7011
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6843
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11594
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9047
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21049
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4706
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3090
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6229
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14726
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Leu57Leu
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum

3-133560484-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560484
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560484
    reference: chr 3
allele count: 1
allele frequency: 8.262823902696986e-6
allele num: 121024
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13655G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.114G>A
  hgvsp: ENST00000486858.1:c.114G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.153G>A
  hgvsp: ENST00000285208.4:c.153G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.54G>A
  hgvsp: ENST00000488969.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.-10G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.153G>A
  hgvsp: ENST00000543906.1:c.153G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.54G>A
  hgvsp: ENST00000477759.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9049
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6944
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11393
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6842
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11602
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4497
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3652
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14713
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu51Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

3-133560513-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560513
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560513
    reference: chr 3
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.130-6T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.31-6T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.130-6T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.91-6T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.-33-6T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13684T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.31-6T>C
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4514
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11333
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9048
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11595
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6288
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6841
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3070
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14058
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3651
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6185
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 3.25e1
  variant carriers: 0
hgvs: c.130-6T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

3-133560529-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560529
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560529
    reference: chr 3
allele count: 1
allele frequency: 8.308546170591069e-6
allele num: 120358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.31-22G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.-33-22G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.91-22G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.31-22G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.130-22G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13700G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.130-22G>A
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10825
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9052
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6840
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11543
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4938
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4657
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12079
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1134
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3650
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ

3-133560531-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560531
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560531
    reference: chr 3
allele count: 1
allele frequency: 8.308822307526131e-6
allele num: 120354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.91-24C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.31-24C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.31-24C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.130-24C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13702C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.-33-24C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.130-24C>T
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9040
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4865
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10801
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6843
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4515
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11496
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1194
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3022
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5953
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

3-133560538-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560538
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560538
    reference: chr 3
allele count: 1
allele frequency: 8.321405984755183e-6
allele num: 120172
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.31-31A>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.-33-31A>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13709A>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.31-31A>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.91-31A>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.130-31A>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.130-31A>C
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6838
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11343
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9034
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4514
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1905
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10198
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2981
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1301
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 702
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3650
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1058
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10513
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 840
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

3-133560539-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560539
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560539
    reference: chr 3
allele count: 1
allele frequency: 8.327365388138501e-6
allele num: 120086
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.130-32G>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.130-32G>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.-33-32G>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.31-32G>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.31-32G>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13710G>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.91-32G>C
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9032
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6838
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11342
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4141
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10196
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 841
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10609
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1311
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4475
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2981
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1046
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 697
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum

3-133560545-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560545
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560545
    reference: chr 3
allele count: 859
allele frequency: 7.156663445196121e-3
allele num: 120028
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.91-38C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13716C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.-33-38C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.31-38C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.130-38C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.130-38C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.31-38C>T
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11094
  bin: 3.25e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 4523
  bin: 4.75e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 2666
  bin: 1.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 2.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 8.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 8973
  bin: 3.75e1
  variant carriers: 106
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 9.75e1
  variant carriers: 75
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 5.75e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 9763
  bin: 2.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 6824
  bin: 4.25e1
  variant carriers: 95
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 6.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 5.25e1
  variant carriers: 83
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 6.25e1
  variant carriers: 42
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1184
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4417
  bin: 8.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1324
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5560
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2929
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9810
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 18
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/3-133560550-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560550
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560550
    reference: chr 3
allele count: 1
allele frequency: 8.340422692622062e-6
allele num: 119898
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.130-43T>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.130-43T>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13721T>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.91-43T>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.31-43T>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.-33-43T>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.31-43T>G
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4513
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3086
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6802
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2784
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10893
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4376
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9204
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1371
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1308
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 696
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1294
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 820
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2952
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20937
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/3-133560553-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560553
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560553
    reference: chr 3
allele count: 2
allele frequency: 1.673948341954167e-5
allele num: 119478
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.130-46G>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13724G>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.130-46G>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.91-46G>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.-33-46G>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.31-46G>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.31-46G>T
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6805
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2784
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4511
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10432
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8658
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1182
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5071
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4516
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2369
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1431
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1642
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

3-133560554-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133560554
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133560554
    reference: chr 3
allele count: 4
allele frequency: 3.34520882466088e-5
allele num: 119574
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.-33-47T>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.96-13725T>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.31-47T>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.130-47T>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.130-47T>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.91-47T>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.31-47T>A
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1894
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8597
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6800
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10202
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2784
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8866
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5748
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1972
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3628
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 769
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1138
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4998
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6110
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1757
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum

3-133583378-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133583378
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133583378
    reference: chr 3
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.90+50C>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.129+50C>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.30+50C>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.30+50C>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.-33-22871C>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.95+84C>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.129+50C>G
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5100
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6652
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4100
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6652
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5240
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6233
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5983
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4921
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4067
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2976
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2281
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1853
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2059
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46592
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2250
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ

3-133583384-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133583384
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133583384
    reference: chr 3
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.129+44T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.90+44T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.129+44T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.30+44T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.-33-22877T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.30+44T>C
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.95+78T>C
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5243
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4921
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5983
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6652
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5099
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2976
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6651
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4067
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2777
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 2290
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2045
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genotype quality: GenotypeQuality
  all individuals: 2313
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

3-133583389-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133583389
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133583389
    reference: chr 3
allele count: 4
allele frequency: 3.294838635277837e-5
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.129+39G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.30+39G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.90+39G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.95+73G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.30+39G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.129+39G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.-33-22882G>A
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5983
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4143
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2294
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5250
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 9.25e1
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genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5099
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6652
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2976
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4067
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4923
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6652
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1502
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1108
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2776
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

3-133583390-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133583390
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133583390
    reference: chr 3
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.95+72A>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.90+38A>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.129+38A>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.129+38A>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.-33-22883A>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.30+38A>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.30+38A>T
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2976
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4921
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6654
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5983
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5251
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4067
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6652
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2300
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2357
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2054
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1503
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: T
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD

3-133583390-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133583390
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133583390
    reference: chr 3
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.90+38A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.30+38A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.30+38A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.-33-22883A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.95+72A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.129+38A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.129+38A>G
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5251
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4067
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6652
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5983
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6654
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2976
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4921
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2779
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
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genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
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: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

3-133583395-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133583395
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133583395
    reference: chr 3
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.30+33C>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.95+67C>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.129+33C>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.90+33C>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.129+33C>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.30+33C>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.-33-22888C>A
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5254
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6652
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5983
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
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genotype depth: GenotypeDepth
  all individuals: 2976
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4921
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6655
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4067
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2054
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 21
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1504
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genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

3-133583397-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133583397
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133583397
    reference: chr 3
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.129+31A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.90+31A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.95+65A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.30+31A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.30+31A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.-33-22890A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.129+31A>G
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5254
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4067
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6655
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2296
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4158
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5983
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genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2976
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4920
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2405
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2052
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1112
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2299
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

3-133583400-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133583400
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133583400
    reference: chr 3
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.-33-22893A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.30+28A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.95+62A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.129+28A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.129+28A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.90+28A>G
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.30+28A>G
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5251
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6653
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2976
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5983
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4918
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4162
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4067
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2787
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1110
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1897
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2301
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

3-133583404-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133583404
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133583404
    reference: chr 3
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.129+24C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.95+58C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.-33-22897C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.30+24C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.129+24C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.90+24C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.30+24C>T
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4918
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4165
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6251
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4067
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6652
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5983
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5253
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2976
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1113
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2416
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2788
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1502
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum

3-133583406-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133583406
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133583406
    reference: chr 3
allele count: 7
allele frequency: 5.765682656826568e-5
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.95+56C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.129+22C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.129+22C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.90+22C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.-33-22899C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.30+22C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.30+22C>T
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4923
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2302
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5253
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5983
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2975
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4067
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4165
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6652
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2053
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2300
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46596
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

3-133583408-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133583408
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133583408
    reference: chr 3
allele count: 3
allele frequency: 2.470966147763776e-5
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.30+20C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.129+20C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.90+20C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.-33-22901C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.30+20C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.129+20C>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.95+54C>T
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5253
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6657
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6252
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4165
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4067
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2975
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5983
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4919
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6653
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2427
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2302
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1503
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2788
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP

3-133583411-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133583411
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133583411
    reference: chr 3
allele count: 3
allele frequency: 2.470966147763776e-5
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.30+17T>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.95+51T>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.129+17T>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.-33-22904T>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.129+17T>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.90+17T>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.30+17T>A
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5255
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6252
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6653
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4166
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6658
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4919
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4067
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5983
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2975
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2788
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2303
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP

3-133583422-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133583422
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133583422
    reference: chr 3
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.129+6G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.95+40G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.129+6G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.-33-22915G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.90+6G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.30+6G>A
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.30+6G>A
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6659
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4168
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4921
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4067
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2313
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5982
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6652
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6254
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1506
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2053
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
hgvs: c.129+6G>A
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/3-133583422-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133583422
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 133583422
    reference: chr 3
allele count: 7
allele frequency: 5.765587678115476e-5
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000417433
  ensembl transcript: ENST00000488969
  gene symbol: RAB6B
  hgvsc: ENST00000488969.1:c.30+6G>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000437797
  ensembl transcript: ENST00000543906
  gene symbol: RAB6B
  hgvsc: ENST00000543906.1:c.129+6G>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000418540
  ensembl transcript: ENST00000469959
  gene symbol: RAB6B
  hgvsc: ENST00000469959.1:c.95+40G>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419941
  ensembl transcript: ENST00000477759
  gene symbol: RAB6B
  hgvsc: ENST00000477759.1:c.30+6G>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000285208
  ensembl transcript: ENST00000285208
  gene symbol: RAB6B
  hgvsc: ENST00000285208.4:c.129+6G>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419526
  ensembl transcript: ENST00000460865
  gene symbol: RAB6B
  hgvsc: ENST00000460865.3:c.-33-22915G>T
  variant of: http://identifiers.org/hgnc/14902
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154917
  ensembl protein: ENSP00000419381
  ensembl transcript: ENST00000486858
  gene symbol: RAB6B
  hgvsc: ENST00000486858.1:c.90+6G>T
  variant of: http://identifiers.org/hgnc/14902
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5982
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2313
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6254
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6652
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4168
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4921
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4067
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6659
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2302
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1506
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46591
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
hgvs: c.129+6G>T
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 469
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3420
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4329
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 234
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 737
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1250
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.057150620414818e-5
allele num: 66246
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16398
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6450
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10298
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e-2

QD
type: SiteQuality
SIO_000300: 1.404e1

MQ
type: SiteQuality
SIO_000300: 5.948e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.45e0

MQRankSum
type: SiteQuality
SIO_000300: 1.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

FS
type: SiteQuality
SIO_000300: 9.350000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.747717e6

GenotypeQuality
all individuals: 23
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10038
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3432
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1250
bin: 9.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6450
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16408
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.699321047526673e-5
allele num: 10310
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 7.52e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.4e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -5.37e-1

DP
type: SiteQuality
SIO_000300: 1.753217e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

QD
type: SiteQuality
SIO_000300: 1.46e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.256e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 545
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10076
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1250
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6462
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508113651444773e-5
allele num: 66308
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.05e0

QD
type: SiteQuality
SIO_000300: 2.945e1

MQRankSum
type: SiteQuality
SIO_000300: 4.26e-1

FS
type: SiteQuality
SIO_000300: 1.8032e1

VQSLOD
type: SiteQuality
SIO_000300: -1.514e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.4e-1

DP
type: SiteQuality
SIO_000300: 1.755032e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

GenotypeQuality
all individuals: 267
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1045
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10163
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1249
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6490
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66400
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.49e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -5.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.37e-1

MQ
type: SiteQuality
SIO_000300: 5.904e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.766726e6

QD
type: SiteQuality
SIO_000300: 1.34e1

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

GenotypeQuality
all individuals: 425
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 6

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6490
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.033695684904695e-5
allele num: 66418
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.768079e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

QD
type: SiteQuality
SIO_000300: 1.356e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.231e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

MQRankSum
type: SiteQuality
SIO_000300: 5.87e-1

FS
type: SiteQuality
SIO_000300: 1.909e0

VQSLOD
type: SiteQuality
SIO_000300: 8.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.455e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2306
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3485
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66588
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.652015919709292e-5
allele num: 11558
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.205e0

FS
type: SiteQuality
SIO_000300: 2.727e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.159e1

MQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e0

DP
type: SiteQuality
SIO_000300: 1.779486e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.21e0

GenotypeQuality
all individuals: 2305
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3799
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10321
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1254
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33690
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 3.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.005104338687885e-5
allele num: 66610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.780603e6

QD
type: SiteQuality
SIO_000300: 1.135e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.53e-1

MQ
type: SiteQuality
SIO_000300: 5.892e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.174e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.02e-1

GenotypeQuality
all individuals: 1254
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3795
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10326
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1048
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
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: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.002191599867904e-5
allele num: 66618
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.437e0

DP
type: SiteQuality
SIO_000300: 1.781045e6

MQRankSum
type: SiteQuality
SIO_000300: 4.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.406e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.92e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

QD
type: SiteQuality
SIO_000300: 1.126e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.28e-1

GenotypeQuality
all individuals: 53
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2302
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3486
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33692
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10327
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4335
bin: 9.75e1
variant carriers: 15

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500960614793468e-5
allele num: 66624
num of homozygotes: 0

South Asian
type: Population
allele count: 14
allele frequency: 8.484848484848485e-4
allele num: 16500
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 5.87e-1

QD
type: SiteQuality
SIO_000300: 1.232e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.76e-1

DP
type: SiteQuality
SIO_000300: 1.781815e6

VQSLOD
type: SiteQuality
SIO_000300: 3.22e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.7e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

GenotypeQuality
all individuals: 33
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33723
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3487
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variant carriers: 0

GenotypeQuality
all individuals: 53
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variant carriers: 0

GenotypeQuality
all individuals: 55
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variant carriers: 0

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

GenotypeQuality
all individuals: 3799
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66630
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.641342074816814e-5
allele num: 10372
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.233e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 9.98e0

DP
type: SiteQuality
SIO_000300: 1.781552e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.23e-1

MQ
type: SiteQuality
SIO_000300: 5.79e1

VQSLOD
type: SiteQuality
SIO_000300: -1.859e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.21e-1

GenotypeQuality
all individuals: 4331
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 10328
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 17
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GenotypeQuality
all individuals: 1256
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variant carriers: 0

GenotypeQuality
all individuals: 37
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variant carriers: 0

GenotypeQuality
all individuals: 3493
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variant carriers: 0

GenotypeQuality
all individuals: 3802
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variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

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

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

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.729206294310911e-4
allele num: 11566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500240038406145e-5
allele num: 66656
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 3.636363636363636e-4
allele num: 16500
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.1e-2

MQ
type: SiteQuality
SIO_000300: 5.924e1

VQSLOD
type: SiteQuality
SIO_000300: 4.22e-1

DP
type: SiteQuality
SIO_000300: 1.783238e6

FS
type: SiteQuality
SIO_000300: 1.815e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.1e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.076e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.14e-1

GenotypeQuality
all individuals: 1048
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 80
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GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 17
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GenotypeQuality
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GenotypeQuality
all individuals: 1253
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 10330
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GenotypeQuality
all individuals: 2308
bin: 8.25e1
variant carriers: 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: 6604
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
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African
type: Population
allele count: 1
allele frequency: 9.637625289128758e-5
allele num: 10376
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66684
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.6e-1

MQ
type: SiteQuality
SIO_000300: 5.865e1

QD
type: SiteQuality
SIO_000300: 1.576e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.902e0

FS
type: SiteQuality
SIO_000300: 3.209e0

DP
type: SiteQuality
SIO_000300: 1.783696e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.77e-1

GenotypeQuality
all individuals: 1048
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 51
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 35
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4322
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GenotypeQuality
all individuals: 3800
bin: 7.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.63948332369385e-5
allele num: 10374
num of homozygotes: 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 (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66676
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.01e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.89e-1

QD
type: SiteQuality
SIO_000300: 8.720000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.141e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.04e-1

FS
type: SiteQuality
SIO_000300: 2.827e0

DP
type: SiteQuality
SIO_000300: 1.783636e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.912e1

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
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 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: 66670
num of homozygotes: 0

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.53e0

FS
type: SiteQuality
SIO_000300: 4.514e0

MQRankSum
type: SiteQuality
SIO_000300: 1.76e0

VQSLOD
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DP
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SIO_000300: 1.783417e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.620000000000001e-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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bin: 6.25e1
variant carriers: 0

Other
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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: 16504
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.000030000300003e-5
allele num: 66666
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.7e-1

FS
type: SiteQuality
SIO_000300: 2.042e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.863e0

QD
type: SiteQuality
SIO_000300: 1.229e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.75e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.32e-1

DP
type: SiteQuality
SIO_000300: 1.783313e6

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
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: 16504
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 6.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.02e0

QD
type: SiteQuality
SIO_000300: 7.85e0

DP
type: SiteQuality
SIO_000300: 1.783127e6

VQSLOD
type: SiteQuality
SIO_000300: -1.753e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.7e-1

MQ
type: SiteQuality
SIO_000300: 5.857e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-2

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: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
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: 16502
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66648
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.021e0

MQ
type: SiteQuality
SIO_000300: 5.914e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.3e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -6.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.879999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.9e-2

DP
type: SiteQuality
SIO_000300: 1.783019e6

QD
type: SiteQuality
SIO_000300: 3.82e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004175804368072e-5
allele num: 66574
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.17e-1

FS
type: SiteQuality
SIO_000300: 1.1528e1

MQRankSum
type: SiteQuality
SIO_000300: 1.8e-1

DP
type: SiteQuality
SIO_000300: 1.779735e6

MQ
type: SiteQuality
SIO_000300: 5.979e1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.188e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

GenotypeQuality
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variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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East Asian
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allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66576
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6590
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South Asian
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allele count: 0
allele frequency: 0.0e0
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
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MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
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
allele num: 11566
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 904
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East Asian
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10366
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.50253929140247e-5
allele num: 66554
num of homozygotes: 0

MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.197e0

MQRankSum
type: SiteQuality
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DP
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InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.62e-1

FS
type: SiteQuality
SIO_000300: 1.777e0

VQSLOD
type: SiteQuality
SIO_000300: 1.13e-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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African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
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Latino
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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
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66444
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East Asian
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South Asian
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allele frequency: 4.24911982517907e-4
allele num: 16474
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
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

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

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

Other
type: Population
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African
type: Population
allele count: 1
allele frequency: 9.658103148541626e-5
allele num: 10354
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Latino
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66446
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ClippingRankSum
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InbreedingCoeff
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FS
type: SiteQuality
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MQRankSum
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VQSLOD
type: SiteQuality
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QD
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BaseQRankSum
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DP
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1247
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 2.75e1
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: 6576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506160195198361e-5
allele num: 66394
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.761545e6

VQSLOD
type: SiteQuality
SIO_000300: -3.78e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.373e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.5e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.76e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.336e1

FS
type: SiteQuality
SIO_000300: 4.514e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.6e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 5
allele frequency: 7.537612687309675e-5
allele num: 66334
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.944e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.385e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.44e-1

DP
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SIO_000300: 1.744791e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.56e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-2

FS
type: SiteQuality
SIO_000300: 3.312e0

QD
type: SiteQuality
SIO_000300: 1.411e1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50993537476596e-5
allele num: 66228
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16438
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

VQSLOD
type: SiteQuality
SIO_000300: -2.873e0

DP
type: SiteQuality
SIO_000300: 1.718049e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.156e0

FS
type: SiteQuality
SIO_000300: 1.2477e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.98e0

MQRankSum
type: SiteQuality
SIO_000300: 1.6e-2

QD
type: SiteQuality
SIO_000300: 1.31e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.092360180333861e-5
allele num: 16414
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66168
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.052e0

MQRankSum
type: SiteQuality
SIO_000300: -1.629e0

FS
type: SiteQuality
SIO_000300: 8.750999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -7.6e-1

DP
type: SiteQuality
SIO_000300: 1.702004e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.933e0

QD
type: SiteQuality
SIO_000300: 1.407e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511761504505049e-5
allele num: 66148
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10314
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16430
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.253e1

MQ
type: SiteQuality
SIO_000300: 5.956e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -7.62e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.700856e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.809e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.23e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.67e-1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4308
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variant carriers: 1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16408
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.714396735962697e-5
allele num: 10294
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66066
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.68e-1

DP
type: SiteQuality
SIO_000300: 1.676833e6

MQRankSum
type: SiteQuality
SIO_000300: -4.84e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.805e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.24e-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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bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66046
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160900859066636e-4
allele num: 8614
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16398
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.031e1

MQRankSum
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BaseQRankSum
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QD
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InbreedingCoeff
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SIO_000300: 1.4e-3

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.42e-1

ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16398
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66046
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160900859066636e-4
allele num: 8614
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.14e-1

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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FS
type: SiteQuality
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VQSLOD
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QD
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MQ
type: SiteQuality
SIO_000300: 6.031e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.39e-1

DP
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.214808515807696e-4
allele num: 65854
num of homozygotes: 0

Other
type: Population
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allele num: 890
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African
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South Asian
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allele count: 1
allele frequency: 6.124448799608035e-5
allele num: 16328
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6544
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.475842891901286e-4
allele num: 11508
num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

Other
type: Population
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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: 6548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65922
num of homozygotes: 0

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

African
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East Asian
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allele count: 1
allele frequency: 1.163873370577281e-4
allele num: 8592
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.46e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.692e0

MQ
type: SiteQuality
SIO_000300: 5.728e1

DP
type: SiteQuality
SIO_000300: 1.657199e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

QD
type: SiteQuality
SIO_000300: 5.37e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

GenotypeQuality
all individuals: 1762
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2381
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3729
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2435
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2180
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1229
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 17544
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7745
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1015
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 15
allele frequency: 9.165342783820114e-4
allele num: 16366
num of homozygotes: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10270
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65744
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.28e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

FS
type: SiteQuality
SIO_000300: 5.98e-1

DP
type: SiteQuality
SIO_000300: 1.654098e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.359e0

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.409999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.432e1

GenotypeQuality
all individuals: 1008
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1015
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2917
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 545
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8045
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1006
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5321
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3605
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.665511265164645e-5
allele num: 11540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.53857791225416e-5
allele num: 66100
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.00133422281521e-4
allele num: 14990
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.1e0

DP
type: SiteQuality
SIO_000300: 2.320057e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.269e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

QD
type: SiteQuality
SIO_000300: 1.15e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.5e-1

FS
type: SiteQuality
SIO_000300: 6.899999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.54e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 247
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5331
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3596
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4575
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 500
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2920
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7971
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2396
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14954
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66074
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.513317191283293e-4
allele num: 6608
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.91e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

DP
type: SiteQuality
SIO_000300: 2.320479e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.63e-1

FS
type: SiteQuality
SIO_000300: 7.35e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.194e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.28e0

MQRankSum
type: SiteQuality
SIO_000300: 1.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

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

GenotypeQuality
all individuals: 553
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2920
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 500
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3596
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7971
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 989
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4341
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4575
bin: 7.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14954
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513454611496201e-5
allele num: 66074
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.28e0

MQRankSum
type: SiteQuality
SIO_000300: 1.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.91e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.63e-1

FS
type: SiteQuality
SIO_000300: 7.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

QD
type: SiteQuality
SIO_000300: 1.194e1

DP
type: SiteQuality
SIO_000300: 2.320479e6

GenotypeQuality
all individuals: 1004
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7971
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 958
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5331
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2396
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22373
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 2920
bin: 7.25e1
variant carriers: 0

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66074
num of homozygotes: 0

South Asian
type: Population
allele count: 15
allele frequency: 1.003076100040123e-3
allele num: 14954
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.91e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.63e-1

FS
type: SiteQuality
SIO_000300: 7.35e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.194e1

DP
type: SiteQuality
SIO_000300: 2.320479e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.33e-1

GenotypeQuality
all individuals: 118
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9642
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4331
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4553
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 918
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2383
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22366
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15098
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.61e-1

FS
type: SiteQuality
SIO_000300: 1.475e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.4e-1

QD
type: SiteQuality
SIO_000300: 1.414e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.64e-1

DP
type: SiteQuality
SIO_000300: 2.328454e6

GenotypeQuality
all individuals: 109
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9892
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2386
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4578
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5451
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22366
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4345
bin: 8.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.313743637204998e-4
allele num: 8644
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15128
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66176
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.330458e6

MQRankSum
type: SiteQuality
SIO_000300: 5.71e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.5e-2

QD
type: SiteQuality
SIO_000300: 1.204e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.14e0

VQSLOD
type: SiteQuality
SIO_000300: 1.54e0

GenotypeQuality
all individuals: 91
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4338
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 162
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1081
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 883
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22360
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3596
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.643201542912247e-5
allele num: 10370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66168
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15142
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.204e0

VQSLOD
type: SiteQuality
SIO_000300: -3.203e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.5e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.732e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

QD
type: SiteQuality
SIO_000300: 1.092e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e0

FS
type: SiteQuality
SIO_000300: 1.4519e1

DP
type: SiteQuality
SIO_000300: 2.331553e6

MQ
type: SiteQuality
SIO_000300: 5.895e1

GenotypeQuality
all individuals: 25805
bin: 9.75e1
variant carriers: 8496

GenotypeQuality
all individuals: 906
bin: 2.25e1
variant carriers: 4

GenotypeQuality
all individuals: 105
bin: 5.25e1
variant carriers: 3

GenotypeQuality
all individuals: 2674
bin: 7.25e1
variant carriers: 6

GenotypeQuality
all individuals: 4111
bin: 7.75e1
variant carriers: 4

GenotypeQuality
all individuals: 169
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2063
bin: 8.75e1
variant carriers: 11

GenotypeQuality
all individuals: 57
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 5209
bin: 6.75e1
variant carriers: 8

GenotypeQuality
all individuals: 3920
bin: 8.25e1
variant carriers: 11

East Asian
type: Population
allele count: 159
allele frequency: 1.838575393154487e-2
allele num: 8648
num of homozygotes: 2

South Asian
type: Population
allele count: 320
allele frequency: 2.072002072002072e-2
allele num: 15444
num of homozygotes: 2

African
type: Population
allele count: 1561
allele frequency: 1.50182797767943e-1
allele num: 10394
num of homozygotes: 116

Other
type: Population
allele count: 63
allele frequency: 7.03125e-2
allele num: 896
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 6097
allele frequency: 9.196910730986213e-2
allele num: 66294
num of homozygotes: 294

Latino
type: Population
allele count: 475
allele frequency: 4.109707561861914e-2
allele num: 11558
num of homozygotes: 8

European (Finnish)
type: Population
allele count: 312
allele frequency: 4.718693284936479e-2
allele num: 6612
num of homozygotes: 8

QD
type: SiteQuality
SIO_000300: 1.413e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.36e-1

FS
type: SiteQuality
SIO_000300: 6.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.68e0

DP
type: SiteQuality
SIO_000300: 2.471641e6

MQRankSum
type: SiteQuality
SIO_000300: 9.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.86e-2

MQ
type: SiteQuality
SIO_000300: 5.966e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.658e0

GenotypeQuality
all individuals: 393
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2379
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 12601
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3651
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 80
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 189
bin: 4.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
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: 1.284686536485098e-4
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 7
allele frequency: 1.055329413538369e-4
allele num: 66330
num of homozygotes: 0

East Asian
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MQRankSum
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FS
type: SiteQuality
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VQSLOD
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MQ
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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QD
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ClippingRankSum
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DP
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.013863773357444e-5
allele num: 66360
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East Asian
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allele frequency: 0.0e0
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VQSLOD
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FS
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DP
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BaseQRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

East Asian
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allele frequency: 0.0e0
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Latino
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South Asian
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allele frequency: 6.205783790492739e-5
allele num: 16114
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.005981903988938e-5
allele num: 66534
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African
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Other
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DP
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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QD
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MQRankSum
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ClippingRankSum
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MQ
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InbreedingCoeff
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SIO_000300: -1.0e-4

FS
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele num: 10404
num of homozygotes: 0

East Asian
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Other
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.502674761074713e-5
allele num: 66548
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South Asian
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Latino
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
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BaseQRankSum
type: SiteQuality
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FS
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MQ
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
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European (Finnish)
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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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European (Non-Finnish)
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allele count: 1
allele frequency: 1.502358703163967e-5
allele num: 66562
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Other
type: Population
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allele num: 904
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FS
type: SiteQuality
SIO_000300: 1.341e1

DP
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VQSLOD
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BaseQRankSum
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MQ
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SIO_000300: 5.973e1

MQRankSum
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.044e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.34e-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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South Asian
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African
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Other
type: Population
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.501997656883655e-5
allele num: 66578
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Latino
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allele frequency: 0.0e0
allele num: 11576
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European (Finnish)
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allele num: 6614
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East Asian
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DP
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MQRankSum
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VQSLOD
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ReadPosRankSum
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QD
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InbreedingCoeff
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BaseQRankSum
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FS
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MQ
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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European (Finnish)
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Latino
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East Asian
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European (Non-Finnish)
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South Asian
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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DP
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InbreedingCoeff
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QD
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MQ
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VQSLOD
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FS
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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Other
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South Asian
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European (Non-Finnish)
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Latino
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East Asian
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BaseQRankSum
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MQRankSum
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FS
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DP
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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MQ
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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African
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South Asian
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Latino
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Other
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European (Finnish)
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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FS
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VQSLOD
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MQ
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ClippingRankSum
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ReadPosRankSum
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QD
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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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European (Finnish)
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African
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South Asian
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Latino
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European (Non-Finnish)
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East Asian
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.36e-1

FS
type: SiteQuality
SIO_000300: 5.876e0

MQRankSum
type: SiteQuality
SIO_000300: 1.07e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.71e0

QD
type: SiteQuality
SIO_000300: 8.289999999999999e0

DP
type: SiteQuality
SIO_000300: 2.335244e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 138
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3650
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 4646
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2371
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12098
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4481
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21043
bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 1
allele frequency: 9.619084263178146e-5
allele num: 10396
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15814
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66424
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 7.13e-1

DP
type: SiteQuality
SIO_000300: 2.333015e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.701e0

MQRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

FS
type: SiteQuality
SIO_000300: 7.12e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.659e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.06e0

QD
type: SiteQuality
SIO_000300: 1.378e1

GenotypeQuality
all individuals: 103
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4477
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
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GenotypeQuality
all individuals: 231
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variant carriers: 0

GenotypeQuality
all individuals: 5729
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4630
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21041
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2369
bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
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: 15712
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: 1
allele frequency: 1.507113576079093e-5
allele num: 66352
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.96e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.13e0

QD
type: SiteQuality
SIO_000300: 1.471e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.57e0

DP
type: SiteQuality
SIO_000300: 2.318097e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.919999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeQuality
all individuals: 111
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21035
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5697
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variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4621
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3649
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2368
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66342
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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.317974e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.569e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.239e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.7e0

QD
type: SiteQuality
SIO_000300: 3.005e1

MQ
type: SiteQuality
SIO_000300: 5.97e1

VQSLOD
type: SiteQuality
SIO_000300: -3.875e0

FS
type: SiteQuality
SIO_000300: 4.51e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.78e-1

GenotypeQuality
all individuals: 776
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 537
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variant carriers: 0

GenotypeQuality
all individuals: 3590
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 21414
bin: 9.75e1
variant carriers: 834

GenotypeQuality
all individuals: 471
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2344
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variant carriers: 0

GenotypeQuality
all individuals: 4541
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 26
allele frequency: 1.664959016393443e-3
allele num: 15616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 130
allele frequency: 1.960429484859452e-3
allele num: 66312
num of homozygotes: 2

African
type: Population
allele count: 633
allele frequency: 6.091224018475751e-2
allele num: 10392
num of homozygotes: 16

Other
type: Population
allele count: 4
allele frequency: 4.524886877828055e-3
allele num: 884
num of homozygotes: 0

Latino
type: Population
allele count: 63
allele frequency: 5.44699982707937e-3
allele num: 11566
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.535833081342606e-4
allele num: 6614
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.424e1

FS
type: SiteQuality
SIO_000300: 7.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.57e-2

DP
type: SiteQuality
SIO_000300: 2.314283e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.61e0

VQSLOD
type: SiteQuality
SIO_000300: 5.43e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.54e-1

GenotypeQuality
all individuals: 4571
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8809
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5539
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variant carriers: 0

GenotypeQuality
all individuals: 4459
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3631
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
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variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1003
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2371
bin: 8.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15536
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508841813024323e-5
allele num: 66276
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.8e0

DP
type: SiteQuality
SIO_000300: 2.295326e6

VQSLOD
type: SiteQuality
SIO_000300: -1.224e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

MQRankSum
type: SiteQuality
SIO_000300: 2.55e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

FS
type: SiteQuality
SIO_000300: 2.565e0

QD
type: SiteQuality
SIO_000300: 1.299e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.16e0

GenotypeQuality
all individuals: 891
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1469
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1334
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
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variant carriers: 0

GenotypeQuality
all individuals: 4447
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20932
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3626
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variant carriers: 0

GenotypeQuality
all individuals: 819
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variant carriers: 0

GenotypeQuality
all individuals: 7153
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2892
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66174
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15262
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.926782273603083e-4
allele num: 10380
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.48e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

FS
type: SiteQuality
SIO_000300: 1.0663e1

MQ
type: SiteQuality
SIO_000300: 5.933e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.822e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.37e0

DP
type: SiteQuality
SIO_000300: 2.286514e6

QD
type: SiteQuality
SIO_000300: 1.555e1

GenotypeQuality
all individuals: 2885
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1364
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1506
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 837
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variant carriers: 0

GenotypeQuality
all individuals: 20935
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 4451
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variant carriers: 0

GenotypeQuality
all individuals: 896
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variant carriers: 0

GenotypeQuality
all individuals: 2371
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4521
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15346
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.042843762274526e-5
allele num: 66194
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.62e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

QD
type: SiteQuality
SIO_000300: 1.411e1

FS
type: SiteQuality
SIO_000300: 3.103e0

DP
type: SiteQuality
SIO_000300: 2.283196e6

BaseQRankSum
type: SiteQuality
SIO_000300: -9.57e-1

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
all individuals: 1093
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variant carriers: 0

GenotypeQuality
all individuals: 2775
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 2286
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
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variant carriers: 0

GenotypeQuality
all individuals: 1497
bin: 8.75e1
variant carriers: 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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
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: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.542487e6

QD
type: SiteQuality
SIO_000300: 1.418e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.88e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

FS
type: SiteQuality
SIO_000300: 1.182e0

VQSLOD
type: SiteQuality
SIO_000300: 1.93e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.652e0

MQRankSum
type: SiteQuality
SIO_000300: 3.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.979e1

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

GenotypeQuality
all individuals: 1498
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variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 34
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1880
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46590
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1105
bin: 7.25e1
variant carriers: 0

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

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

European (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: 10406
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.03e-1

QD
type: SiteQuality
SIO_000300: 7.82e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.985e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.02e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.64e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.99e-1

DP
type: SiteQuality
SIO_000300: 3.543017e6

GenotypeQuality
all individuals: 2353
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2050
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1882
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46595
bin: 9.75e1
variant carriers: 4

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

GenotypeQuality
all individuals: 2295
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.993946114424431e-5
allele num: 66734
num of homozygotes: 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
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

QD
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FS
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MQ
type: SiteQuality
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MQRankSum
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 1.0e-4

DP
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ReadPosRankSum
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SIO_000300: 1.05e0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

DP
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FS
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InbreedingCoeff
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QD
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MQ
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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VQSLOD
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GenotypeQuality
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bin: 5.25e1
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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East Asian
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66736
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Other
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num of homozygotes: 0

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

BaseQRankSum
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ReadPosRankSum
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QD
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VQSLOD
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FS
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InbreedingCoeff
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MQ
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MQRankSum
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DP
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ClippingRankSum
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

East Asian
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South Asian
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Other
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num of homozygotes: 0

FS
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
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DP
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MQ
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MQRankSum
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VQSLOD
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QD
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

Latino
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allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

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

South Asian
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

VQSLOD
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MQRankSum
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FS
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QD
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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DP
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MQ
type: SiteQuality
SIO_000300: 5.99e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.94e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

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

African
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allele frequency: 0.0e0
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East Asian
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Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

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

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

MQ
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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QD
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VQSLOD
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FS
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MQRankSum
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

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

African
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Latino
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East Asian
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allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

Other
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num of homozygotes: 0

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

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

African
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num of homozygotes: 0

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

South Asian
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Other
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Latino
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European (Finnish)
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East Asian
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allele frequency: 6.933210076265311e-4
allele num: 8654
num of homozygotes: 0

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

East Asian
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European (Finnish)
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European (Non-Finnish)
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Other
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African
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Latino
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South Asian
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QD
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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FS
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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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Latino
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South Asian
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European (Finnish)
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African
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East Asian
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European (Non-Finnish)
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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MQ
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ReadPosRankSum
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FS
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ClippingRankSum
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QD
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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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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2434
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1907
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2790
bin: 9.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.973e1

QD
type: SiteQuality
SIO_000300: 1.231e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 5.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.02e-1

DP
type: SiteQuality
SIO_000300: 3.54445e6

VQSLOD
type: SiteQuality
SIO_000300: 3.83e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.352e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.08e-1