9-69205574-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69205574
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69205574
    reference: chr 9
allele count: 1
allele frequency: 1.104923539291081e-5
allele num: 90504
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.964A>G
  hgvsp: ENSP00000366677.5:p.Ile322Val
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1602A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2153A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2152A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2734A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1615A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.904A>G
  hgvsp: ENSP00000371836.4:p.Ile302Val
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1211A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.856A>G
  hgvsp: ENSP00000366668.1:p.Ile286Val
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.2007A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.*1106A>G
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1983
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4303
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11463
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9303
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22575
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile322Val
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/9-69205580-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69205580
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69205580
    reference: chr 9
allele count: 1
allele frequency: 1.284785569288486e-5
allele num: 77834
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.850G>T
  hgvsp: ENSP00000366668.1:p.Val284Leu
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1596G>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.958G>T
  hgvsp: ENSP00000366677.5:p.Val320Leu
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1609G>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.898G>T
  hgvsp: ENSP00000371836.4:p.Val300Leu
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.2001G>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2728G>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.*1100G>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2146G>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2147G>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1205G>T
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6848
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18813
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11634
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12401
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6585
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13994
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val320Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

9-69205581-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69205581
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69205581
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 77698
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1608G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.957G>A
  hgvsp: ENST00000377457.5:c.957G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2145G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1204G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2146G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.*1099G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.897G>A
  hgvsp: ENST00000382399.4:c.897G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.849G>A
  hgvsp: ENST00000377449.1:c.849G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1595G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2727G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.2000G>A
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6554
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6890
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12351
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18840
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11627
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu319Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum

9-69205585-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69205585
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69205585
    reference: chr 9
allele count: 1
allele frequency: 1.752418337305482e-5
allele num: 57064
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.893G>A
  hgvsp: ENSP00000371836.4:p.Gly298Glu
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.953G>A
  hgvsp: ENSP00000366677.5:p.Gly318Glu
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1591G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.*1095G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1200G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2142G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.845G>A
  hgvsp: ENSP00000366668.1:p.Gly282Glu
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2723G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2141G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.1996G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1604G>A
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11476
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14989
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9803
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13088
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly318Glu
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD

9-69205602-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69205602
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69205602
    reference: chr 9
allele count: 5
allele frequency: 8.101101749837978e-4
allele num: 6172
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1590-16A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1199-16A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.*1078A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.1979A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2141-16A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.892-16A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2140-16A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2722-16A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.952-16A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.844-16A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1603-16A>G
  variant of: http://identifiers.org/hgnc/31978
canonical: false
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31934
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4278
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

9-69206699-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206699
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206699
    reference: chr 9
allele count: 9
allele frequency: 2.25e-1
allele num: 40
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1198+35C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.843+35C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.951+35C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1589+35C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1602+35C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.891+35C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.882C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2721+35C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.261C>T
  hgvsp: ENSP00000408279.1:p.Ser88Phe
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2139+35C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2140+35C>T
  variant of: http://identifiers.org/hgnc/31978
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 2.5e0
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 8
hgvs: p.Ser88Phe
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: African
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

9-69206794-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206794
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206794
    reference: chr 9
allele count: 1
allele frequency: 9.09090909090909e-3
allele num: 110
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.787T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2079T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.831T>C
  hgvsp: ENST00000382399.4:c.831T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.891T>C
  hgvsp: ENST00000377457.5:c.891T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1542T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2080T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.166T>C
  hgvsp: ENST00000416428.1:c.166T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2661T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.783T>C
  hgvsp: ENST00000377449.1:c.783T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1138T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1529T>C
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4608
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu297Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

9-69206867-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206867
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206867
    reference: chr 9
allele count: 4
allele frequency: 3.90625e-3
allele num: 1024
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1132+36A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2073+36A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2655+36A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.825+36A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.777+36A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1536+36A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1523+36A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2074+36A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.781+36A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.160+36A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.885+36A>G
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6926
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum

http://identifiers.org/exac.variant/9-69206880-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206880
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206880
    reference: chr 9
allele count: 12
allele frequency: 1.736111111111111e-3
allele num: 6912
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1132+23T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1523+23T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.777+23T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2655+23T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.160+23T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2074+23T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.825+23T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1536+23T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.781+23T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.885+23T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2073+23T>G
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 25947
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 24127
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21885
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/9-69206890-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206890
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206890
    reference: chr 9
allele count: 1
allele frequency: 3.184916236702975e-5
allele num: 31398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1536+13T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2655+13T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.777+13T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.781+13T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.885+13T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2073+13T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1132+13T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1523+13T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.825+13T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.160+13T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2074+13T>G
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7465
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13770
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

9-69206893-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206893
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206893
    reference: chr 9
allele count: 1
allele frequency: 2.529212403257626e-5
allele num: 39538
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2074+10A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1536+10A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1523+10A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.825+10A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.160+10A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2073+10A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.777+10A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1132+10A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.781+10A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.885+10A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2655+10A>G
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5624
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17759
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

9-69206895-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206895
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206895
    reference: chr 9
allele count: 1
allele frequency: 2.207115741149466e-5
allele num: 45308
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1132+8C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1536+8C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.825+8C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2074+8C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.885+8C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1523+8C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.781+8C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.160+8C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2073+8C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.777+8C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2655+8C>T
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20502
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4658
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.885+8C>T
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

9-69206898-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206898
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206898
    reference: chr 9
allele count: 1
allele frequency: 1.82395213949586e-5
allele num: 54826
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2655+5A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2074+5A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.160+5A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.825+5A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1523+5A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1132+5A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1536+5A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.885+5A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2073+5A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.781+5A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.777+5A>G
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 25796
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3550
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24777
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.885+5A>G
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/9-69206901-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206901
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206901
    reference: chr 9
allele count: 1
allele frequency: 1.590431961320695e-5
allele num: 62876
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2655+2T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.885+2T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1523+2T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.777+2T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.781+2T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.825+2T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.160+2T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1132+2T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2074+2T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1536+2T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2073+2T>G
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: splice donor
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28551
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22552
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
hgvs: c.885+2T>G
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

9-69206912-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206912
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206912
    reference: chr 9
allele count: 1
allele frequency: 1.187535626068782e-5
allele num: 84208
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.768G>A
  hgvsp: ENSP00000366668.1:p.Met256Ile
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.816G>A
  hgvsp: ENSP00000371836.4:p.Met272Ile
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.876G>A
  hgvsp: ENSP00000366677.5:p.Met292Ile
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2064G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2065G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.772G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1514G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1527G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2646G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.151G>A
  hgvsp: ENSP00000408279.1:p.Met51Ile
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1123G>A
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38465
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13290
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met292Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

9-69206913-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206913
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206913
    reference: chr 9
allele count: 1
allele frequency: 1.169919041602321e-5
allele num: 85476
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1122T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1513T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.150T>A
  hgvsp: ENSP00000408279.1:p.Met51Lys
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.815T>A
  hgvsp: ENSP00000371836.4:p.Met272Lys
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.875T>A
  hgvsp: ENSP00000366677.5:p.Met292Lys
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2645T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1526T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.767T>A
  hgvsp: ENSP00000366668.1:p.Met256Lys
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.771T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2063T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2064T>A
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12722
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met292Lys
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum

9-69206914-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206914
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206914
    reference: chr 9
allele count: 1
allele frequency: 1.154521104645793e-5
allele num: 86616
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.770A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.149A>G
  hgvsp: ENSP00000408279.1:p.Met51Val
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1121A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1512A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.766A>G
  hgvsp: ENSP00000366668.1:p.Met256Val
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2062A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2644A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1525A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.814A>G
  hgvsp: ENSP00000371836.4:p.Met272Val
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2063A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.874A>G
  hgvsp: ENSP00000366677.5:p.Met292Val
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12227
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39617
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met292Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: T
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

9-69206916-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206916
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206916
    reference: chr 9
allele count: 82
allele frequency: 9.257795741413959e-4
allele num: 88574
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2060A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.768A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.812A>G
  hgvsp: ENSP00000371836.4:p.Asn271Ser
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2061A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.872A>G
  hgvsp: ENSP00000366677.5:p.Asn291Ser
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1510A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.764A>G
  hgvsp: ENSP00000366668.1:p.Asn255Ser
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1119A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.147A>G
  hgvsp: ENSP00000408279.1:p.Asn50Ser
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1523A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2642A>G
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11323
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 40508
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asn291Ser
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/9-69206921-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206921
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206921
    reference: chr 9
allele count: 2
allele frequency: 2.161414429602732e-5
allele num: 92532
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1505T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.142T>G
  hgvsp: ENSP00000408279.1:p.His48Gln
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1114T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.763T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2056T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.867T>G
  hgvsp: ENSP00000366677.5:p.His289Gln
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.807T>G
  hgvsp: ENSP00000371836.4:p.His269Gln
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.759T>G
  hgvsp: ENSP00000366668.1:p.His253Gln
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1518T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2055T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2637T>G
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9547
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42139
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His289Gln
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

9-69206924-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206924
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206924
    reference: chr 9
allele count: 50099
allele frequency: 4.803171498696119e-1
allele num: 104304
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1515A>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1111A>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2634A>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.804A>T
  hgvsp: ENSP00000371836.4:p.Glu268Asp
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2053A>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.139A>T
  hgvsp: ENSP00000408279.1:p.Glu47Asp
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.864A>T
  hgvsp: ENSP00000366677.5:p.Glu288Asp
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.756A>T
  hgvsp: ENSP00000366668.1:p.Glu252Asp
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1502A>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.760A>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2052A>T
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: missense
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 8.75e1
  variant carriers: 502
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 6.75e1
  variant carriers: 1308
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 8.25e1
  variant carriers: 621
genotype depth: GenotypeDepth
  all individuals: 2194
  bin: 5.75e1
  variant carriers: 2187
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 6.25e1
  variant carriers: 1712
genotype depth: GenotypeDepth
  all individuals: 2624
  bin: 1.25e1
  variant carriers: 2118
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 2.5e0
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 2904
  bin: 5.25e1
  variant carriers: 2891
genotype depth: GenotypeDepth
  all individuals: 6092
  bin: 2.75e1
  variant carriers: 5833
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 7.5e0
  variant carriers: 673
genotype depth: GenotypeDepth
  all individuals: 4421
  bin: 1.75e1
  variant carriers: 4062
genotype depth: GenotypeDepth
  all individuals: 7158
  bin: 2.25e1
  variant carriers: 5183
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 7.75e1
  variant carriers: 763
genotype depth: GenotypeDepth
  all individuals: 5799
  bin: 3.25e1
  variant carriers: 5659
genotype depth: GenotypeDepth
  all individuals: 4508
  bin: 4.25e1
  variant carriers: 4478
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 7.25e1
  variant carriers: 980
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 9.25e1
  variant carriers: 410
genotype depth: GenotypeDepth
  all individuals: 5226
  bin: 3.75e1
  variant carriers: 5163
genotype depth: GenotypeDepth
  all individuals: 3696
  bin: 4.75e1
  variant carriers: 3678
genotype depth: GenotypeDepth
  all individuals: 2768
  bin: 9.75e1
  variant carriers: 2763
genotype quality: GenotypeQuality
hgvs: p.Glu288Asp
num of homozygotes: 182
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

9-69206930-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206930
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206930
    reference: chr 9
allele count: 1
allele frequency: 9.569011712470337e-6
allele num: 104504
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2046G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1105G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.798G>A
  hgvsp: ENST00000382399.4:c.798G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1496G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2628G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.754G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2047G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.750G>A
  hgvsp: ENST00000377449.1:c.750G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.858G>A
  hgvsp: ENST00000377457.5:c.858G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.133G>A
  hgvsp: ENST00000416428.1:c.133G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1509G>A
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4757
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3827
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11628
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10705
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys286Lys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum

9-69206934-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206934
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206934
    reference: chr 9
allele count: 1
allele frequency: 9.559132795472795e-6
allele num: 104612
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2624C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2043C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.750C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1492C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.854C>T
  hgvsp: ENSP00000366677.5:p.Ala285Val
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.129C>T
  hgvsp: ENSP00000408279.1:p.Ala44Val
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1101C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.746C>T
  hgvsp: ENSP00000366668.1:p.Ala249Val
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.794C>T
  hgvsp: ENSP00000371836.4:p.Ala265Val
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1505C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2042C>T
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2691
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12403
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3771
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10701
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17529
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4749
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala285Val
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

9-69206935-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206935
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206935
    reference: chr 9
allele count: 1
allele frequency: 9.559132795472795e-6
allele num: 104612
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2041G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.749G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2623G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1491G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.745G>A
  hgvsp: ENSP00000366668.1:p.Ala249Thr
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.793G>A
  hgvsp: ENSP00000371836.4:p.Ala265Thr
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.853G>A
  hgvsp: ENSP00000366677.5:p.Ala285Thr
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1100G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.128G>A
  hgvsp: ENSP00000408279.1:p.Ala44Thr
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1504G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2042G>A
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17531
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12430
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2703
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10678
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3782
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala285Thr
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

9-69206940-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206940
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206940
    reference: chr 9
allele count: 5
allele frequency: 4.790097909601272e-5
allele num: 104382
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.848G>A
  hgvsp: ENSP00000366677.5:p.Gly283Glu
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.788G>A
  hgvsp: ENSP00000371836.4:p.Gly263Glu
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.740G>A
  hgvsp: ENSP00000366668.1:p.Gly247Glu
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2618G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.123G>A
  hgvsp: ENSP00000408279.1:p.Gly42Glu
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1095G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.744G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2036G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1499G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2037G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1486G>A
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17595
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10638
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12013
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3849
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4746
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly283Glu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP

9-69206947-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206947
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206947
    reference: chr 9
allele count: 26
allele frequency: 2.516015405755869e-4
allele num: 103338
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2611G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.116G>A
  hgvsp: ENSP00000408279.1:p.Val40Ile
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.733G>A
  hgvsp: ENSP00000366668.1:p.Val245Ile
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.841G>A
  hgvsp: ENSP00000366677.5:p.Val281Ile
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2030G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.781G>A
  hgvsp: ENSP00000371836.4:p.Val261Ile
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1088G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2029G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1479G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.737G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1492G>A
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 17558
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4138
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10614
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9776
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4752
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
hgvs: p.Val281Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

9-69206959-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206959
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206959
    reference: chr 9
allele count: 2
allele frequency: 1.975503753457132e-5
allele num: 101240
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2017A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.725A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1480A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.829A>G
  hgvsp: ENSP00000366677.5:p.Ile277Val
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.104A>G
  hgvsp: ENSP00000408279.1:p.Ile36Val
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.721A>G
  hgvsp: ENSP00000366668.1:p.Ile241Val
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.769A>G
  hgvsp: ENSP00000371836.4:p.Ile257Val
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2599A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2018A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1467A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1076A>G
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4627
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10135
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4689
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10150
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14889
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5482
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile277Val
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

9-69206960-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206960
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206960
    reference: chr 9
allele count: 3
allele frequency: 2.968651044965168e-5
allele num: 101056
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.103A>G
  hgvsp: ENST00000416428.1:c.103A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.724A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2598A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.720A>G
  hgvsp: ENST00000377449.1:c.720A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2016A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1466A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.828A>G
  hgvsp: ENST00000377457.5:c.828A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1075A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.768A>G
  hgvsp: ENST00000382399.4:c.768A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2017A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1479A>G
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1622
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4637
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10666
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4679
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14498
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10099
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5170
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr276Thr
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS

9-69206961-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206961
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206961
    reference: chr 9
allele count: 1
allele frequency: 9.920438086545901e-6
allele num: 100802
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1478C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.102C>G
  hgvsp: ENSP00000408279.1:p.Thr35Arg
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.719C>G
  hgvsp: ENSP00000366668.1:p.Thr240Arg
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2015C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1074C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2016C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1465C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.723C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.767C>G
  hgvsp: ENSP00000371836.4:p.Thr256Arg
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.827C>G
  hgvsp: ENSP00000366677.5:p.Thr276Arg
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2597C>G
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 11217
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14107
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4803
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4646
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4673
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr276Arg
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: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum

9-69206963-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206963
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206963
    reference: chr 9
allele count: 1
allele frequency: 9.955994504291034e-6
allele num: 100442
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2595T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.721T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.100T>C
  hgvsp: ENST00000416428.1:c.100T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.825T>C
  hgvsp: ENST00000377457.5:c.825T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.717T>C
  hgvsp: ENST00000377449.1:c.717T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2014T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.765T>C
  hgvsp: ENST00000382399.4:c.765T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1463T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1072T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2013T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1476T>C
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1818
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4055
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4703
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4654
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12487
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13124
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val275Val
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

9-69206964-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206964
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206964
    reference: chr 9
allele count: 42
allele frequency: 4.191784103157811e-4
allele num: 100196
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.716T>A
  hgvsp: ENSP00000366668.1:p.Val239Asp
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2012T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1462T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1071T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2594T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.720T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.99T>A
  hgvsp: ENSP00000408279.1:p.Val34Asp
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.764T>A
  hgvsp: ENSP00000371836.4:p.Val255Asp
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.824T>A
  hgvsp: ENSP00000366677.5:p.Val275Asp
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2013T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1475T>A
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 13152
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9768
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4707
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3746
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4649
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1894
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12537
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Val275Asp
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum

9-69206965-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206965
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206965
    reference: chr 9
allele count: 2
allele frequency: 2.001280819724624e-5
allele num: 99936
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2012G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.719G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1474G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2593G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.763G>A
  hgvsp: ENSP00000371836.4:p.Val255Ile
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1461G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.715G>A
  hgvsp: ENSP00000366668.1:p.Val239Ile
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2011G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1070G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.98G>A
  hgvsp: ENSP00000408279.1:p.Val34Ile
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.823G>A
  hgvsp: ENSP00000366677.5:p.Val275Ile
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11902
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4712
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2746
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13825
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9669
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val275Ile
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

9-69206966-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206966
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206966
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 99136
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1069T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2592T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.822T>C
  hgvsp: ENST00000377457.5:c.822T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1473T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.718T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.97T>C
  hgvsp: ENST00000416428.1:c.97T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.714T>C
  hgvsp: ENST00000377449.1:c.714T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2010T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2011T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.762T>C
  hgvsp: ENST00000382399.4:c.762T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1460T>C
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15864
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4699
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2686
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3800
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9754
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4603
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile274Ile
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

9-69206968-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206968
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206968
    reference: chr 9
allele count: 6
allele frequency: 6.057424383152284e-5
allele num: 99052
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1458A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.712A>G
  hgvsp: ENSP00000366668.1:p.Ile238Val
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2590A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2008A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1471A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.820A>G
  hgvsp: ENSP00000366677.5:p.Ile274Val
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1067A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.95A>G
  hgvsp: ENSP00000408279.1:p.Ile33Val
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.760A>G
  hgvsp: ENSP00000371836.4:p.Ile254Val
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.716A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2009A>G
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4718
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2671
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9016
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15888
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4596
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile274Val
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/9-69206981-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206981
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206981
    reference: chr 9
allele count: 1
allele frequency: 1.215125887041897e-5
allele num: 82296
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.757-10T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2005-10T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2587-10T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.713-10T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2006-10T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1458T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.817-10T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.709-10T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1455-10T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.92-10T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1064-10T>G
  variant of: http://identifiers.org/hgnc/31978
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17409
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13473
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5241
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11556
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

9-69206986-AAAT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206986
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206983
    reference: chr 9
allele count: 2
allele frequency: 3.356831151393085e-5
allele num: 59580
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1455-18_1455-16delATT
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2587-18_2587-16delATT
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1450_1452delATT
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.817-18_817-16delATT
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2005-18_2005-16delATT
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2006-18_2006-16delATT
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.757-18_757-16delATT
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.713-18_713-16delATT
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.92-18_92-16delATT
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.709-18_709-16delATT
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1064-18_1064-16delATT
  variant of: http://identifiers.org/hgnc/31978
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 12978
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4508
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16936
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4999
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10425
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 8.25e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: AAAT
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

9-69206989-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206989
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206989
    reference: chr 9
allele count: 1
allele frequency: 2.009484768105458e-5
allele num: 49764
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.92-18A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.757-18A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2587-18A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1455-18A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1064-18A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.709-18A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2006-18A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2005-18A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.817-18A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1450A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.713-18A>G
  variant of: http://identifiers.org/hgnc/31978
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4136
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8802
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12621
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4738
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18718
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1802
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/9-69206990-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69206990
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69206990
    reference: chr 9
allele count: 1
allele frequency: 2.006742655321882e-5
allele num: 49832
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.709-19T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.757-19T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1449T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2587-19T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2006-19T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.817-19T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2005-19T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.713-19T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1064-19T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1455-19T>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.92-19T>G
  variant of: http://identifiers.org/hgnc/31978
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8791
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18744
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4749
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12600
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD

9-69207009-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69207009
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69207009
    reference: chr 9
allele count: 9
allele frequency: 4.677754677754678e-3
allele num: 1924
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2587-38C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2006-38C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.92-38C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1064-38C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1455-38C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.817-38C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1430C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.757-38C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.709-38C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.713-38C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2005-38C>T
  variant of: http://identifiers.org/hgnc/31978
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.5e0
  variant carriers: 133
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 2.5e0
  variant carriers: 313
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.75e1
  variant carriers: 6
num of homozygotes: 4
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum

9-69207017-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69207017
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69207017
    reference: chr 9
allele count: 1
allele frequency: 3.912363067292645e-4
allele num: 2556
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.713-46A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2006-46A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.817-46A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.709-46A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1455-46A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2587-46A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000498101
  gene symbol: CBWD6
  hgvsc: ENST00000498101.1:n.1422A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.757-46A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1064-46A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.92-46A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2005-46A>G
  variant of: http://identifiers.org/hgnc/31978
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

9-69218472-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69218472
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69218472
    reference: chr 9
allele count: 1
allele frequency: 6.211180124223603e-4
allele num: 1610
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.712+38A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.91+38A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2586+38A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1063+38A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.816+38A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1454+38A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2005+38A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.756+38A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.708+38A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2004+38A>G
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6512
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

9-69218480-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69218480
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69218480
    reference: chr 9
allele count: 7
allele frequency: 5.035971223021582e-3
allele num: 1390
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1454+30T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.756+30T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2005+30T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.712+30T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2004+30T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.816+30T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1063+30T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2586+30T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.708+30T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.91+30T>C
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20594
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5712
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

9-69218487-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69218487
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69218487
    reference: chr 9
allele count: 6
allele frequency: 4.010695187165776e-3
allele num: 1496
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2586+23C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.756+23C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1454+23C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.91+23C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2005+23C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.816+23C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.708+23C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1063+23C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.712+23C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2004+23C>T
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17549
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: Latino
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

9-69218514-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69218514
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69218514
    reference: chr 9
allele count: 1
allele frequency: 5.336179295624333e-4
allele num: 1874
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.87A>G
  hgvsp: ENSP00000408279.1:p.Asp30Gly
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.2000A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2582A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.704A>G
  hgvsp: ENSP00000366668.1:p.Asp235Gly
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.812A>G
  hgvsp: ENSP00000366677.5:p.Asp271Gly
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.2001A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1059A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.708A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.752A>G
  hgvsp: ENSP00000371836.4:p.Asp251Gly
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1450A>G
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29706
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2774
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2479
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp271Gly
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

9-69218523-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69218523
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69218523
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 1914
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.743C>T
  hgvsp: ENSP00000371836.4:p.Pro248Leu
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.699C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.695C>T
  hgvsp: ENSP00000366668.1:p.Pro232Leu
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1050C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.1992C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.1991C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1441C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.78C>T
  hgvsp: ENSP00000408279.1:p.Pro27Leu
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.803C>T
  hgvsp: ENSP00000366677.5:p.Pro268Leu
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2573C>T
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30613
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro268Leu
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

9-69218548-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69218548
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69218549
    reference: chr 9
allele count: 1
allele frequency: 5.197505197505198e-4
allele num: 1924
alternate allele: GT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1415dupA
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.717dupA
  hgvsp: ENSP00000371836.4:p.Leu240ThrfsTer12
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.673dupA
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2547dupA
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.669dupA
  hgvsp: ENSP00000366668.1:p.Leu224ThrfsTer12
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.1965dupA
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.1966dupA
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.52dupA
  hgvsp: ENSP00000408279.1:p.Leu19ThrfsTer12
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1024dupA
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.777dupA
  hgvsp: ENSP00000366677.5:p.Leu260ThrfsTer12
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27386
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu260ThrfsTer12
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

9-69218556-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69218556
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69218556
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 1968
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.45A>C
  hgvsp: ENSP00000408279.1:p.Gln16Pro
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.1958A>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.666A>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2540A>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.662A>C
  hgvsp: ENSP00000366668.1:p.Gln221Pro
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.710A>C
  hgvsp: ENSP00000371836.4:p.Gln237Pro
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.1959A>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1408A>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1017A>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.770A>C
  hgvsp: ENSP00000366677.5:p.Gln257Pro
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 25016
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25033
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1432
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gln257Pro
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

9-69218590-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69218590
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69218590
    reference: chr 9
allele count: 1
allele frequency: 5.235602094240838e-4
allele num: 1910
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.1954-29T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.765-29T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2535-29T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1403-29T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1012-29T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.1953-29T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.632T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.705-29T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.657-29T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.40-29T>C
  variant of: http://identifiers.org/hgnc/31978
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5631
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

9-69218592-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69218592
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69218592
    reference: chr 9
allele count: 7
allele frequency: 3.812636165577342e-3
allele num: 1836
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.1953-31C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000477430
  gene symbol: CBWD6
  hgvsc: ENST00000477430.1:n.630C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2535-31C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1403-31C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1012-31C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.705-31C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.765-31C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.657-31C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.40-31C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.1954-31C>A
  variant of: http://identifiers.org/hgnc/31978
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5332
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

9-69229598-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69229598
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69229598
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 1146
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.1953+14G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468061
  gene symbol: CBWD6
  hgvsc: ENST00000468061.1:n.2534+14G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1402+14G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.656+14G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.1011+14G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.764+14G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.704+14G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.1952+14G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000408279
  ensembl transcript: ENST00000416428
  gene symbol: CBWD6
  hgvsc: ENST00000416428.1:c.39+14G>A
  variant of: http://identifiers.org/hgnc/31978
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

9-69238113-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69238113
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69238113
    reference: chr 9
allele count: 2
allele frequency: 9.44733112895607e-5
allele num: 21170
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.831+117G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.602+117G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000494632
  gene symbol: CBWD6
  hgvsc: ENST00000494632.1:n.215+117G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461834
  gene symbol: CBWD6
  hgvsc: ENST00000461834.1:n.339G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.554+117G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.1727+117G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.662+117G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000485382
  gene symbol: CBWD6
  hgvsc: ENST00000485382.2:n.377+117G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.786+1900G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000377445
  gene symbol: CBWD6
  hgvsc: ENST00000377445.5:n.852G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1083+117G>A
  variant of: http://identifiers.org/hgnc/31978
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23524
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23041
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5996
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1389
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum

9-69238114-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69238114
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69238114
    reference: chr 9
allele count: 1
allele frequency: 4.668970025212438e-5
allele num: 21418
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000377445
  gene symbol: CBWD6
  hgvsc: ENST00000377445.5:n.851C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.602+116C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.831+116C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.554+116C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.786+1899C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.1727+116C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461834
  gene symbol: CBWD6
  hgvsc: ENST00000461834.1:n.338C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000485382
  gene symbol: CBWD6
  hgvsc: ENST00000485382.2:n.377+116C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.662+116C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1083+116C>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000494632
  gene symbol: CBWD6
  hgvsc: ENST00000494632.1:n.215+116C>T
  variant of: http://identifiers.org/hgnc/31978
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23566
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6078
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22975
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

9-69238120-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69238120
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69238120
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 21868
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.554+110C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000485382
  gene symbol: CBWD6
  hgvsc: ENST00000485382.2:n.377+110C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.1727+110C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.662+110C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1083+110C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000377445
  gene symbol: CBWD6
  hgvsc: ENST00000377445.5:n.845C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.831+110C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461834
  gene symbol: CBWD6
  hgvsc: ENST00000461834.1:n.332C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.602+110C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000494632
  gene symbol: CBWD6
  hgvsc: ENST00000494632.1:n.215+110C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.786+1893C>G
  variant of: http://identifiers.org/hgnc/31978
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25297
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6223
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21282
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2016
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

9-69238127-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69238127
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69238127
    reference: chr 9
allele count: 1
allele frequency: 4.221190375685944e-5
allele num: 23690
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000494632
  gene symbol: CBWD6
  hgvsc: ENST00000494632.1:n.215+103C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.1727+103C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.554+103C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.831+103C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000485382
  gene symbol: CBWD6
  hgvsc: ENST00000485382.2:n.377+103C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461834
  gene symbol: CBWD6
  hgvsc: ENST00000461834.1:n.325C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.786+1886C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1083+103C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.602+103C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000377445
  gene symbol: CBWD6
  hgvsc: ENST00000377445.5:n.838C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.662+103C>G
  variant of: http://identifiers.org/hgnc/31978
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6260
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17047
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29008
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

9-69238127-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69238127
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69238127
    reference: chr 9
allele count: 1
allele frequency: 4.221190375685944e-5
allele num: 23690
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000485382
  gene symbol: CBWD6
  hgvsc: ENST00000485382.2:n.377+103C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.662+103C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1083+103C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461834
  gene symbol: CBWD6
  hgvsc: ENST00000461834.1:n.325C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.831+103C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.554+103C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000377445
  gene symbol: CBWD6
  hgvsc: ENST00000377445.5:n.838C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.1727+103C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.786+1886C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000494632
  gene symbol: CBWD6
  hgvsc: ENST00000494632.1:n.215+103C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.602+103C>A
  variant of: http://identifiers.org/hgnc/31978
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17047
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29008
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6260
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

9-69238131-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69238131
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69238131
    reference: chr 9
allele count: 1
allele frequency: 3.937317899047169e-5
allele num: 25398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000485382
  gene symbol: CBWD6
  hgvsc: ENST00000485382.2:n.377+99T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000377445
  gene symbol: CBWD6
  hgvsc: ENST00000377445.5:n.834T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.1727+99T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.831+99T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461834
  gene symbol: CBWD6
  hgvsc: ENST00000461834.1:n.321T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.662+99T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.554+99T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.786+1882T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.602+99T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000494632
  gene symbol: CBWD6
  hgvsc: ENST00000494632.1:n.215+99T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1083+99T>C
  variant of: http://identifiers.org/hgnc/31978
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 14333
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6065
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2117
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

9-69238132-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69238132
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69238132
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 25698
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.662+98G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.602+98G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.831+98G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1083+98G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000485382
  gene symbol: CBWD6
  hgvsc: ENST00000485382.2:n.377+98G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461834
  gene symbol: CBWD6
  hgvsc: ENST00000461834.1:n.320G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000494632
  gene symbol: CBWD6
  hgvsc: ENST00000494632.1:n.215+98G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000377445
  gene symbol: CBWD6
  hgvsc: ENST00000377445.5:n.833G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.786+1881G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.1727+98G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.554+98G>A
  variant of: http://identifiers.org/hgnc/31978
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13757
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6025
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3082
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31506
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

9-69238137-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69238137
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69238137
    reference: chr 9
allele count: 1
allele frequency: 3.478502852372339e-5
allele num: 28748
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.831+93A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461834
  gene symbol: CBWD6
  hgvsc: ENST00000461834.1:n.315A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000494632
  gene symbol: CBWD6
  hgvsc: ENST00000494632.1:n.215+93A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.662+93A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.554+93A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1083+93A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000485382
  gene symbol: CBWD6
  hgvsc: ENST00000485382.2:n.377+93A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.1727+93A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.602+93A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000377445
  gene symbol: CBWD6
  hgvsc: ENST00000377445.5:n.828A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.786+1876A>G
  variant of: http://identifiers.org/hgnc/31978
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5459
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32859
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

9-69238145-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69238145
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69238145
    reference: chr 9
allele count: 2
allele frequency: 5.356473297980609e-5
allele num: 37338
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000485382
  gene symbol: CBWD6
  hgvsc: ENST00000485382.2:n.377+85C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461834
  gene symbol: CBWD6
  hgvsc: ENST00000461834.1:n.307C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.662+85C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.602+85C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.1727+85C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000377445
  gene symbol: CBWD6
  hgvsc: ENST00000377445.5:n.820C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000494632
  gene symbol: CBWD6
  hgvsc: ENST00000494632.1:n.215+85C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.786+1868C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.554+85C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.831+85C>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1083+85C>G
  variant of: http://identifiers.org/hgnc/31978
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4372
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32977
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

9-69238146-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69238146
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69238146
    reference: chr 9
allele count: 64
allele frequency: 1.57775367320777e-3
allele num: 40564
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000494632
  gene symbol: CBWD6
  hgvsc: ENST00000494632.1:n.215+84A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.786+1867A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.831+84A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000485382
  gene symbol: CBWD6
  hgvsc: ENST00000485382.2:n.377+84A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461834
  gene symbol: CBWD6
  hgvsc: ENST00000461834.1:n.306A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.662+84A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.554+84A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.602+84A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000377445
  gene symbol: CBWD6
  hgvsc: ENST00000377445.5:n.819A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.1727+84A>G
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1083+84A>G
  variant of: http://identifiers.org/hgnc/31978
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6103
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4012
  bin: 1.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 1.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32489
  bin: 7.5e0
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 12013
  bin: 2.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 2.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 5762
  bin: 7.5e0
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

9-69238163-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69238163
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69238163
    reference: chr 9
allele count: 2
allele frequency: 1.88821752265861e-5
allele num: 105920
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000494632
  gene symbol: CBWD6
  hgvsc: ENST00000494632.1:n.215+67A>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.831+67A>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.662+67A>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461834
  gene symbol: CBWD6
  hgvsc: ENST00000461834.1:n.289A>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.554+67A>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.602+67A>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000485382
  gene symbol: CBWD6
  hgvsc: ENST00000485382.2:n.377+67A>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.1727+67A>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1083+67A>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000377445
  gene symbol: CBWD6
  hgvsc: ENST00000377445.5:n.802A>T
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.786+1850A>T
  variant of: http://identifiers.org/hgnc/31978
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1149
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

9-69238166-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69238166
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69238166
    reference: chr 9
allele count: 1
allele frequency: 9.105146228648432e-6
allele num: 109828
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000494632
  gene symbol: CBWD6
  hgvsc: ENST00000494632.1:n.215+64C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461834
  gene symbol: CBWD6
  hgvsc: ENST00000461834.1:n.286C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1083+64C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.831+64C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000377445
  gene symbol: CBWD6
  hgvsc: ENST00000377445.5:n.799C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.554+64C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.786+1847C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.662+64C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000485382
  gene symbol: CBWD6
  hgvsc: ENST00000485382.2:n.377+64C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.602+64C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.1727+64C>A
  variant of: http://identifiers.org/hgnc/31978
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3772
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4252
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45128
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

9-69238171-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69238171
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69238171
    reference: chr 9
allele count: 3
allele frequency: 2.653129808797778e-5
allele num: 113074
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000377445
  gene symbol: CBWD6
  hgvsc: ENST00000377445.5:n.794T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000485382
  gene symbol: CBWD6
  hgvsc: ENST00000485382.2:n.377+59T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.662+59T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.831+59T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.602+59T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000494632
  gene symbol: CBWD6
  hgvsc: ENST00000494632.1:n.215+59T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461834
  gene symbol: CBWD6
  hgvsc: ENST00000461834.1:n.281T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.554+59T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.1727+59T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.786+1842T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1083+59T>C
  variant of: http://identifiers.org/hgnc/31978
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4488
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 46416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1626
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum

9-69238176-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69238176
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69238176
    reference: chr 9
allele count: 55431
allele frequency: 4.78645689416966e-1
allele num: 115808
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000494632
  gene symbol: CBWD6
  hgvsc: ENST00000494632.1:n.215+54G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.1727+54G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.662+54G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461834
  gene symbol: CBWD6
  hgvsc: ENST00000461834.1:n.276G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.786+1837G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.554+54G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.602+54G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.831+54G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000377445
  gene symbol: CBWD6
  hgvsc: ENST00000377445.5:n.789G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000485382
  gene symbol: CBWD6
  hgvsc: ENST00000485382.2:n.377+54G>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1083+54G>A
  variant of: http://identifiers.org/hgnc/31978
canonical: false
consequence: non coding transcript exon
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 4785
  bin: 6.25e1
  variant carriers: 4774
genotype depth: GenotypeDepth
  all individuals: 3106
  bin: 7.75e1
  variant carriers: 3095
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 8.75e1
  variant carriers: 1831
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 7.25e1
  variant carriers: 3720
genotype depth: GenotypeDepth
  all individuals: 3334
  bin: 3.75e1
  variant carriers: 3294
genotype depth: GenotypeDepth
  all individuals: 3108
  bin: 2.25e1
  variant carriers: 889
genotype depth: GenotypeDepth
  all individuals: 3983
  bin: 4.25e1
  variant carriers: 3936
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 2.75e1
  variant carriers: 1409
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 1.75e1
  variant carriers: 551
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 2.5e0
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 4731
  bin: 4.75e1
  variant carriers: 4695
genotype depth: GenotypeDepth
  all individuals: 4429
  bin: 6.75e1
  variant carriers: 4423
genotype depth: GenotypeDepth
  all individuals: 6459
  bin: 9.75e1
  variant carriers: 6432
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 1.25e1
  variant carriers: 306
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 7.5e0
  variant carriers: 185
genotype depth: GenotypeDepth
  all individuals: 5078
  bin: 5.75e1
  variant carriers: 5052
genotype depth: GenotypeDepth
  all individuals: 4979
  bin: 5.25e1
  variant carriers: 4953
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 8.25e1
  variant carriers: 2425
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 3.25e1
  variant carriers: 2187
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 9.25e1
  variant carriers: 1314
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 4.75e1
  variant carriers: 68
num of homozygotes: 196
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: C
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

9-69238177-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69238177
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69238177
    reference: chr 9
allele count: 1
allele frequency: 8.525003836251726e-6
allele num: 117302
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.1727+53T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000377445
  gene symbol: CBWD6
  hgvsc: ENST00000377445.5:n.788T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.831+53T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.662+53T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.602+53T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.786+1836T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1083+53T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000485382
  gene symbol: CBWD6
  hgvsc: ENST00000485382.2:n.377+53T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461834
  gene symbol: CBWD6
  hgvsc: ENST00000461834.1:n.275T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000494632
  gene symbol: CBWD6
  hgvsc: ENST00000494632.1:n.215+53T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.554+53T>A
  variant of: http://identifiers.org/hgnc/31978
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4748
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4931
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4834
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4504
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7152
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3006
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2604
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2490
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum

9-69238180-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69238180
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69238180
    reference: chr 9
allele count: 1
allele frequency: 8.519919571959241e-6
allele num: 117372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.554+50G>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.662+50G>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461834
  gene symbol: CBWD6
  hgvsc: ENST00000461834.1:n.272G>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000377445
  gene symbol: CBWD6
  hgvsc: ENST00000377445.5:n.785G>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.1727+50G>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1083+50G>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000494632
  gene symbol: CBWD6
  hgvsc: ENST00000494632.1:n.215+50G>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.602+50G>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.786+1833G>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000485382
  gene symbol: CBWD6
  hgvsc: ENST00000485382.2:n.377+50G>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.831+50G>C
  variant of: http://identifiers.org/hgnc/31978
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4932
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4380
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3707
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4834
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4504
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7152
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4748
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2603
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

9-69238191-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69238191
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69238191
    reference: chr 9
allele count: 10
allele frequency: 8.493001766544368e-5
allele num: 117744
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.786+1822T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1083+39T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.602+39T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000485382
  gene symbol: CBWD6
  hgvsc: ENST00000485382.2:n.377+39T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000377445
  gene symbol: CBWD6
  hgvsc: ENST00000377445.5:n.774T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.662+39T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.1727+39T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461834
  gene symbol: CBWD6
  hgvsc: ENST00000461834.1:n.261T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000494632
  gene symbol: CBWD6
  hgvsc: ENST00000494632.1:n.215+39T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.554+39T>C
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.831+39T>C
  variant of: http://identifiers.org/hgnc/31978
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4934
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4749
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4833
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4503
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2603
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3938
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7155
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3711
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

9-69238193-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69238193
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69238193
    reference: chr 9
allele count: 1
allele frequency: 8.489396743467409e-6
allele num: 117794
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461834
  gene symbol: CBWD6
  hgvsc: ENST00000461834.1:n.259T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000494632
  gene symbol: CBWD6
  hgvsc: ENST00000494632.1:n.215+37T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.786+1820T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.602+37T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.662+37T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000377445
  gene symbol: CBWD6
  hgvsc: ENST00000377445.5:n.772T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000485382
  gene symbol: CBWD6
  hgvsc: ENST00000485382.2:n.377+37T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.831+37T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1083+37T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.1727+37T>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.554+37T>A
  variant of: http://identifiers.org/hgnc/31978
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2603
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4748
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3989
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4833
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4504
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4934
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7155
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3712
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

9-69238196-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69238196
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 69238196
    reference: chr 9
allele count: 2
allele frequency: 1.696727013590783e-5
allele num: 117874
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000371836
  ensembl transcript: ENST00000382399
  gene symbol: CBWD6
  hgvsc: ENST00000382399.4:c.602+34C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000495626
  gene symbol: CBWD6
  hgvsc: ENST00000495626.2:n.831+34C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366668
  ensembl transcript: ENST00000377449
  gene symbol: CBWD6
  hgvsc: ENST00000377449.1:c.554+34C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461834
  gene symbol: CBWD6
  hgvsc: ENST00000461834.1:n.256C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000377445
  gene symbol: CBWD6
  hgvsc: ENST00000377445.5:n.769C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000466320
  gene symbol: CBWD6
  hgvsc: ENST00000466320.1:n.786+1817C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000494632
  gene symbol: CBWD6
  hgvsc: ENST00000494632.1:n.215+34C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl protein: ENSP00000366677
  ensembl transcript: ENST00000377457
  gene symbol: CBWD6
  hgvsc: ENST00000377457.5:c.662+34C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000468763
  gene symbol: CBWD6
  hgvsc: ENST00000468763.2:n.1083+34C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000461037
  gene symbol: CBWD6
  hgvsc: ENST00000461037.2:n.1727+34C>A
  variant of: http://identifiers.org/hgnc/31978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204790
  ensembl transcript: ENST00000485382
  gene symbol: CBWD6
  hgvsc: ENST00000485382.2:n.377+34C>A
  variant of: http://identifiers.org/hgnc/31978
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4045
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4748
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2604
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4934
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3712
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4505
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7155
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4833
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 6898
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 120
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 9870
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1294
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35539
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2999
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 767
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51264
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11654
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.410835214446952e-4
allele num: 7088
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7208
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7460
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5172
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.079e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.11e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 6.47e0

DP
type: SiteQuality
SIO_000300: 8.04528e5

ClippingRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e-1

MQ
type: SiteQuality
SIO_000300: 3.236e1

GenotypeQuality
all individuals: 4405
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 611
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3215
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1427
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32892
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4538
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 548
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6222
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6052
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.242253015830306e-5
allele num: 44598
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6420
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.38261e5

MQRankSum
type: SiteQuality
SIO_000300: 5.45e-1

FS
type: SiteQuality
SIO_000300: 6.368e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.8e-2

MQ
type: SiteQuality
SIO_000300: 3.316e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.21e-1

QD
type: SiteQuality
SIO_000300: 9.66e0

VQSLOD
type: SiteQuality
SIO_000300: -4.595e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.59e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.45e-1

GenotypeQuality
all individuals: 1352
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 589
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 432
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33065
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3158
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4433
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14096
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 9.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6038
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44514
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4538
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 544
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6212
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9448
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 2.162e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.24e-1

MQ
type: SiteQuality
SIO_000300: 3.052e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.713e0

VQSLOD
type: SiteQuality
SIO_000300: -4.401e0

DP
type: SiteQuality
SIO_000300: 7.37439e5

MQRankSum
type: SiteQuality
SIO_000300: 5.82e-1

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

GenotypeDepth
all individuals: 5139
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1227
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 396
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2453
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1288
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23337
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24376
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 451
bin: 2.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2497
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5052
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 434
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33180
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4996
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3844
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3320
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.603077909586406e-4
allele num: 6238
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.953e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.45e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.41e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.42e0

MQ
type: SiteQuality
SIO_000300: 3.149e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.15e-2

QD
type: SiteQuality
SIO_000300: 1.597e1

FS
type: SiteQuality
SIO_000300: 2.431e0

DP
type: SiteQuality
SIO_000300: 6.53875e5

VQSLOD
type: SiteQuality
SIO_000300: -4.684e0

GenotypeQuality
all individuals: 3402
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28154
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 4197
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 97
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 265
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 32
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 988
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 213
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1206
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 52
bin: 7.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 74
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3788
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 4.8828125e-3
allele num: 1024
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 538
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 368
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 3.09e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.82e-2

QD
type: SiteQuality
SIO_000300: 1.115e1

FS
type: SiteQuality
SIO_000300: 7.928e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQRankSum
type: SiteQuality
SIO_000300: -4.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.64e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.084e0

DP
type: SiteQuality
SIO_000300: 1.70779e5

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 3

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

GenotypeQuality
all individuals: 22
bin: 2.25e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 355
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 7

GenotypeQuality
all individuals: 663
bin: 7.5e0
variant carriers: 18

GenotypeQuality
all individuals: 2
bin: 7.75e1
variant carriers: 2

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

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

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

GenotypeQuality
all individuals: 12
bin: 6.25e1
variant carriers: 6

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

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 7

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

Latino
type: Population
allele count: 1
allele frequency: 5.0e-1
allele num: 2
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 4.444444444444444e-1
allele num: 18
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.812e3

VQSLOD
type: SiteQuality
SIO_000300: -4.112e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.76e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

MQ
type: SiteQuality
SIO_000300: 2.253e1

QD
type: SiteQuality
SIO_000300: 1.265e1

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.75e1
variant carriers: 1

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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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African
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South Asian
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European (Non-Finnish)
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East Asian
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Latino
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VQSLOD
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MQRankSum
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InbreedingCoeff
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MQ
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FS
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QD
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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East Asian
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Other
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ClippingRankSum
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DP
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VQSLOD
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MQ
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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FS
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QD
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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East Asian
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Latino
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South Asian
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African
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European (Non-Finnish)
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MQRankSum
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BaseQRankSum
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MQ
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DP
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FS
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InbreedingCoeff
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QD
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 202
num of homozygotes: 0

East Asian
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Latino
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allele frequency: 2.627430373095113e-4
allele num: 3806
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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 frequency: 0.0e0
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South Asian
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African
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BaseQRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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FS
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MQ
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MQRankSum
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QD
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

East Asian
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South Asian
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African
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Other
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Latino
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allele frequency: 2.02757502027575e-4
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European (Non-Finnish)
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QD
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MQRankSum
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InbreedingCoeff
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MQ
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FS
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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Other
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African
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European (Finnish)
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European (Non-Finnish)
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South Asian
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East Asian
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QD
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DP
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ReadPosRankSum
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MQRankSum
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MQ
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BaseQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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Other
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European (Finnish)
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European (Non-Finnish)
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South Asian
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East Asian
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FS
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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QD
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VQSLOD
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BaseQRankSum
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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European (Finnish)
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African
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Other
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35428
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.8e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e-1

MQ
type: SiteQuality
SIO_000300: 3.204e1

DP
type: SiteQuality
SIO_000300: 8.20649e5

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.21e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.106e0

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

GenotypeQuality
all individuals: 284
bin: 3.75e1
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.096348161502662e-5
allele num: 47702
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6340
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4664
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9028
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 598
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8816
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7060
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 3.56e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.087e0

MQRankSum
type: SiteQuality
SIO_000300: 1.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 7.36e0

DP
type: SiteQuality
SIO_000300: 9.81905e5

ClippingRankSum
type: SiteQuality
SIO_000300: -3.62e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.087e0

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9064
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4742
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48376
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.404099971918001e-4
allele num: 7122
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9154
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 612
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.198e0

QD
type: SiteQuality
SIO_000300: 2.29e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e0

MQ
type: SiteQuality
SIO_000300: 3.2e1

FS
type: SiteQuality
SIO_000300: 3.746e0

VQSLOD
type: SiteQuality
SIO_000300: -4.166e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-3

DP
type: SiteQuality
SIO_000300: 9.91353e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

MQRankSum
type: SiteQuality
SIO_000300: 3.04e-1

GenotypeQuality
all individuals: 34698
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 250
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variant carriers: 0

GenotypeQuality
all individuals: 817
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variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48960
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.083188908145581e-4
allele num: 9232
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7188
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4826
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6474
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9310
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.000065e6

FS
type: SiteQuality
SIO_000300: 1.855e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.175e0

MQRankSum
type: SiteQuality
SIO_000300: -3.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.96e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

QD
type: SiteQuality
SIO_000300: 1.48e0

MQ
type: SiteQuality
SIO_000300: 3.191e1

VQSLOD
type: SiteQuality
SIO_000300: -5.278e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.04e-1

GenotypeQuality
all individuals: 261
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 235
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variant carriers: 1

GenotypeQuality
all individuals: 34
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GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
all individuals: 110
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variant carriers: 0

GenotypeQuality
all individuals: 1458
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GenotypeQuality
all individuals: 566
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variant carriers: 1

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
all individuals: 34
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variant carriers: 1

GenotypeQuality
all individuals: 65
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variant carriers: 0

GenotypeQuality
all individuals: 4553
bin: 6.75e1
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GenotypeQuality
all individuals: 712
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variant carriers: 1

GenotypeQuality
all individuals: 319
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GenotypeQuality
all individuals: 386
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GenotypeQuality
all individuals: 463
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variant carriers: 68

GenotypeQuality
all individuals: 35522
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GenotypeQuality
all individuals: 11079
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variant carriers: 2

GenotypeQuality
all individuals: 108
bin: 4.25e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9734
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 640
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7286
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.0e-5
allele num: 50000
num of homozygotes: 0

African
type: Population
allele count: 76
allele frequency: 1.155015197568389e-2
allele num: 6580
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 5.33731853116994e-4
allele num: 9368
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4966
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-3

FS
type: SiteQuality
SIO_000300: 1.328e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.24e-1

MQ
type: SiteQuality
SIO_000300: 3.155e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.61e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.287e0

DP
type: SiteQuality
SIO_000300: 1.017443e6

QD
type: SiteQuality
SIO_000300: 4.62e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.98e-1

GenotypeQuality
all individuals: 4753
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variant carriers: 0

GenotypeQuality
all individuals: 540
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 654
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GenotypeQuality
all individuals: 465
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.469723691945914e-4
allele num: 6804
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5286
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7456
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52034
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9678
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.425070688030161e-5
allele num: 10610
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 3.283e1

VQSLOD
type: SiteQuality
SIO_000300: -4.247e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.33e-1

MQRankSum
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SIO_000300: 1.08e0

QD
type: SiteQuality
SIO_000300: 1.284e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.4e-2

FS
type: SiteQuality
SIO_000300: 3.079e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

DP
type: SiteQuality
SIO_000300: 1.049799e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-2

GenotypeQuality
all individuals: 299
bin: 4.25e1
variant carriers: 264

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 170

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 544
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GenotypeQuality
all individuals: 278
bin: 1.25e1
variant carriers: 167

GenotypeQuality
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variant carriers: 451

GenotypeQuality
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bin: 4.75e1
variant carriers: 346

GenotypeQuality
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bin: 6.25e1
variant carriers: 462

GenotypeQuality
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variant carriers: 404

GenotypeQuality
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variant carriers: 499

GenotypeQuality
all individuals: 44606
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variant carriers: 44604

GenotypeQuality
all individuals: 505
bin: 9.25e1
variant carriers: 505

South Asian
type: Population
allele count: 6517
allele frequency: 4.765979230656721e-1
allele num: 13674
num of homozygotes: 10

European (Finnish)
type: Population
allele count: 2925
allele frequency: 4.836309523809524e-1
allele num: 6048
num of homozygotes: 4

Other
type: Population
allele count: 371
allele frequency: 4.907407407407408e-1
allele num: 756
num of homozygotes: 1

African
type: Population
allele count: 3515
allele frequency: 4.659331919406151e-1
allele num: 7544
num of homozygotes: 14

Latino
type: Population
allele count: 5314
allele frequency: 4.968212415856395e-1
allele num: 10696
num of homozygotes: 56

East Asian
type: Population
allele count: 3221
allele frequency: 4.20825712045989e-1
allele num: 7654
num of homozygotes: 11

European (Non-Finnish)
type: Population
allele count: 28236
allele frequency: 4.873990195401505e-1
allele num: 57932
num of homozygotes: 86

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 3.17e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.0938e2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.72e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.3e-2

DP
type: SiteQuality
SIO_000300: 2.282494e6

QD
type: SiteQuality
SIO_000300: 8.640000000000001e0

GenotypeQuality
all individuals: 309
bin: 9.75e1
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
all individuals: 27
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 262
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GenotypeQuality
all individuals: 504
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GenotypeQuality
all individuals: 8015
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GenotypeQuality
all individuals: 1827
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GenotypeQuality
all individuals: 915
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GenotypeQuality
all individuals: 321
bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13818
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.725744658820281e-5
allele num: 57946
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6068
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7546
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7790
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.656e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

MQ
type: SiteQuality
SIO_000300: 3.167e1

DP
type: SiteQuality
SIO_000300: 1.507876e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.01e-1

QD
type: SiteQuality
SIO_000300: 1.629e1

FS
type: SiteQuality
SIO_000300: 1.603e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.99e-1

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
all individuals: 27
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GenotypeQuality
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GenotypeQuality
all individuals: 1059
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.724375775969099e-5
allele num: 57992
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7546
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10572
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6088
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 3.231e1

MQRankSum
type: SiteQuality
SIO_000300: 1.33e-1

BaseQRankSum
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SIO_000300: -1.46e-1

VQSLOD
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SIO_000300: -3.899e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: -6.27e-1

QD
type: SiteQuality
SIO_000300: 6.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

DP
type: SiteQuality
SIO_000300: 1.512134e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.51e-1

GenotypeQuality
all individuals: 91
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7552
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.724911167074896e-5
allele num: 57974
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13844
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7820
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6086
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

MQRankSum
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SIO_000300: 7.61e-1

MQ
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SIO_000300: 3.176e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.58e-1

DP
type: SiteQuality
SIO_000300: 1.511894e6

ClippingRankSum
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SIO_000300: -8.500000000000001e-2

FS
type: SiteQuality
SIO_000300: 1.052e0

VQSLOD
type: SiteQuality
SIO_000300: -4.28e0

BaseQRankSum
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SIO_000300: -1.212e0

QD
type: SiteQuality
SIO_000300: 3.48e0

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13780
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.640652542079978e-5
allele num: 57866
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7816
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7554
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6050
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.95e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.14e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -3.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.14e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

MQ
type: SiteQuality
SIO_000300: 3.16e1

VQSLOD
type: SiteQuality
SIO_000300: -4.211e0

DP
type: SiteQuality
SIO_000300: 1.506902e6

GenotypeQuality
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bin: 4.25e1
variant carriers: 1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 17

GenotypeQuality
all individuals: 1682
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.743679163034002e-5
allele num: 57350
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5966
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 4.443127962085308e-4
allele num: 13504
num of homozygotes: 0

East Asian
type: Population
allele count: 8
allele frequency: 1.026430587631511e-3
allele num: 7794
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.545628102329134e-5
allele num: 10476
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 1.333333333333333e-3
allele num: 7500
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.95e-1

MQ
type: SiteQuality
SIO_000300: 3.204e1

VQSLOD
type: SiteQuality
SIO_000300: -2.922e0

DP
type: SiteQuality
SIO_000300: 1.481997e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 3.868e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.6e-2

QD
type: SiteQuality
SIO_000300: 2.836e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.47e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 105
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.581977794990963e-4
allele num: 7746
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56268
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7368
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13018
num of homozygotes: 0

Latino
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: 5804
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 3.18e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

MQRankSum
type: SiteQuality
SIO_000300: 3.47e-1

BaseQRankSum
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SIO_000300: 9.77e-1

DP
type: SiteQuality
SIO_000300: 1.38378e6

VQSLOD
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SIO_000300: -4.086e0

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.358695652173913e-4
allele num: 7360
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7736
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5792
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12970
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 720
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.559605595699996e-5
allele num: 56186
num of homozygotes: 0

BaseQRankSum
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SIO_000300: 1.35e-1

MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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DP
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QD
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MQ
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VQSLOD
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ClippingRankSum
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56042
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5770
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10278
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.29366106080207e-4
allele num: 7730
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 12914
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7350
num of homozygotes: 0

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

InbreedingCoeff
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BaseQRankSum
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MQ
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SIO_000300: 3.147e1

FS
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ClippingRankSum
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QD
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DP
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VQSLOD
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ReadPosRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 89
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.797878976918278e-5
allele num: 12824
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7318
num of homozygotes: 0

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

East Asian
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allele 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

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

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

InbreedingCoeff
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SIO_000300: -5.2e-3

MQ
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SIO_000300: 3.311e1

MQRankSum
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ClippingRankSum
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FS
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VQSLOD
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ReadPosRankSum
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QD
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BaseQRankSum
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SIO_000300: 2.2e0

DP
type: SiteQuality
SIO_000300: 1.336802e6

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 32

GenotypeQuality
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variant carriers: 3

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

Latino
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allele count: 2
allele frequency: 1.954652071931196e-4
allele num: 10232
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 2.511751408374897e-4
allele num: 55738
num of homozygotes: 0

Other
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num of homozygotes: 0

South Asian
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allele frequency: 2.036021926389977e-3
allele num: 12770
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 7708
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 3.179e1

VQSLOD
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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QD
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DP
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FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -1.72e-1

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

South Asian
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allele count: 1
allele frequency: 7.866582756450598e-5
allele num: 12712
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5720
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.798367082688919e-5
allele num: 55606
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.18e-1

MQ
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VQSLOD
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SIO_000300: -4.208e0

QD
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MQRankSum
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SIO_000300: 7.89e-1

InbreedingCoeff
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SIO_000300: -5.8e-3

FS
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SIO_000300: 2.448e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.39e-1

DP
type: SiteQuality
SIO_000300: 1.307981e6

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7212
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 702
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10152
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 12462
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7682
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55236
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5690
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.557e0

MQ
type: SiteQuality
SIO_000300: 3.173e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.7e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.92e0

MQRankSum
type: SiteQuality
SIO_000300: 9.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.22e-1

QD
type: SiteQuality
SIO_000300: 5.13e0

DP
type: SiteQuality
SIO_000300: 1.256107e6

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12436
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 1.087114074503551e-4
allele num: 55192
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7680
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7216
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10142
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5684
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Other
type: Population
allele count: 0
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allele num: 702
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e-2

QD
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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SIO_000300: 8.8e-1

FS
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InbreedingCoeff
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SIO_000300: -6.8e-3

MQRankSum
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DP
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MQ
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SIO_000300: 3.232e1

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

Latino
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allele count: 1
allele frequency: 1.116071428571429e-4
allele num: 8960
num of homozygotes: 0

Other
type: Population
allele count: 0
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allele num: 550
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South Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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MQ
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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Latino
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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: 5.990176111177669e-5
allele num: 33388
num of homozygotes: 0

African
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Other
type: Population
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allele num: 402
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MQRankSum
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DP
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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FS
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QD
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InbreedingCoeff
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BaseQRankSum
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MQ
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SIO_000300: 3.18e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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allele frequency: 2.264492753623188e-4
allele num: 4416
num of homozygotes: 0

South Asian
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Latino
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allele frequency: 0.0e0
allele num: 6072
num of homozygotes: 0

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

African
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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: 2662
num of homozygotes: 0

QD
type: SiteQuality
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BaseQRankSum
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DP
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MQRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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FS
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ClippingRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

GenotypeQuality
all individuals: 16589
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2760
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 112
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1207
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1382
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3496
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22373
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 844
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 57
bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3440
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4418
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4988
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6074
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2674
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.583972475091391e-5
allele num: 27902
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.8e-2

QD
type: SiteQuality
SIO_000300: 5.6e0

MQRankSum
type: SiteQuality
SIO_000300: -8.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-2

MQ
type: SiteQuality
SIO_000300: 3.26e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.25e-1

DP
type: SiteQuality
SIO_000300: 6.77335e5

FS
type: SiteQuality
SIO_000300: 2.754e0

VQSLOD
type: SiteQuality
SIO_000300: -3.95e0

GenotypeQuality
all individuals: 123
bin: 1.25e1
variant carriers: 108

GenotypeQuality
all individuals: 10
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 546
bin: 2.5e0
variant carriers: 16

GenotypeQuality
all individuals: 327
bin: 7.5e0
variant carriers: 197

GenotypeQuality
all individuals: 73
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 19
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 6.25e1
variant carriers: 3

GenotypeQuality
all individuals: 92
bin: 1.75e1
variant carriers: 80

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

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

GenotypeQuality
all individuals: 123
bin: 3.25e1
variant carriers: 6

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 128
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 2.25e1
variant carriers: 30

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 63
bin: 6.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 5.780346820809249e-4
allele num: 1730
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.25e-1
allele num: 64
num of homozygotes: 4

MQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

MQ
type: SiteQuality
SIO_000300: 2.456e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.953e-1

DP
type: SiteQuality
SIO_000300: 3.3805e4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.5609e2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.2e-1

QD
type: SiteQuality
SIO_000300: 2.266e1

FS
type: SiteQuality
SIO_000300: 2.6526e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

GenotypeQuality
all individuals: 94
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 177
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 26
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 598
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 9.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 156
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 3.571428571428571e-2
allele num: 28
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 554
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1760
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.78e-2

FS
type: SiteQuality
SIO_000300: 2.522e0

DP
type: SiteQuality
SIO_000300: 4.2682e4

MQ
type: SiteQuality
SIO_000300: 2.745e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.424e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.6e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.808e0

QD
type: SiteQuality
SIO_000300: 5.1e0

GenotypeQuality
all individuals: 787
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 106
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
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variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 122
num of homozygotes: 0

European (Non-Finnish)
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: 94
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.762430939226519e-3
allele num: 362
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 128
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.31e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.54e-1

MQ
type: SiteQuality
SIO_000300: 3.237e1

VQSLOD
type: SiteQuality
SIO_000300: -1.018e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.0929e4

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.6e-2

QD
type: SiteQuality
SIO_000300: 1.213e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.122e-1

GenotypeQuality
all individuals: 286
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 15076
bin: 7.5e0
variant carriers: 4

GenotypeQuality
all individuals: 11
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 830
bin: 2.25e1
variant carriers: 2

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

GenotypeQuality
all individuals: 101
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 77
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 9
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.263157894736842e-3
allele num: 760
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 6.211180124223602e-3
allele num: 322
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 84
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.09090909090909e-3
allele num: 110
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

QD
type: SiteQuality
SIO_000300: 7.51e0

VQSLOD
type: SiteQuality
SIO_000300: -1.392e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.659999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.88e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.108e-1

DP
type: SiteQuality
SIO_000300: 6.676e4

MQ
type: SiteQuality
SIO_000300: 3.076e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

GenotypeQuality
all individuals: 253
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1026
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4702
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 60
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 3.25e1
variant carriers: 0

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 3.694581280788177e-3
allele num: 812
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 106
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 5.813953488372093e-3
allele num: 344
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.064516129032258e-3
allele num: 124
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.894e0

MQRankSum
type: SiteQuality
SIO_000300: -1.537e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 6.45e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.749e0

DP
type: SiteQuality
SIO_000300: 7.2018e4

MQ
type: SiteQuality
SIO_000300: 3.118e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.023e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 71
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 63
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28454
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 80
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variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1213
bin: 2.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 20
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 148
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.304147465437788e-3
allele num: 434
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1024
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 104
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.64e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.77e0

MQ
type: SiteQuality
SIO_000300: 3.172e1

MQRankSum
type: SiteQuality
SIO_000300: -1.034e0

DP
type: SiteQuality
SIO_000300: 1.01419e5

QD
type: SiteQuality
SIO_000300: 3.49e0

VQSLOD
type: SiteQuality
SIO_000300: -2.352e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.78e-1

GenotypeQuality
all individuals: 29863
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 56
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2782
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variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 62
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variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 7.25e1
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GenotypeQuality
all individuals: 806
bin: 2.5e0
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GenotypeQuality
all individuals: 184
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 561
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variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 156
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 434
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1056
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 124
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 102
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.22e-1

QD
type: SiteQuality
SIO_000300: 6.02e0

MQRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

MQ
type: SiteQuality
SIO_000300: 3.11e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.63e0

DP
type: SiteQuality
SIO_000300: 1.06927e5

ClippingRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

InbreedingCoeff
type: SiteQuality
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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Other
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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QD
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FS
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InbreedingCoeff
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DP
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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MQRankSum
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MQ
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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European (Finnish)
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East Asian
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Other
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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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European (Non-Finnish)
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allele frequency: 0.0e0
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DP
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InbreedingCoeff
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QD
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ClippingRankSum
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FS
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MQRankSum
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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South Asian
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Other
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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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European (Non-Finnish)
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allele frequency: 8.865248226950354e-4
allele num: 1128
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FS
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SIO_000300: 0.0e0

MQRankSum
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MQ
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BaseQRankSum
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DP
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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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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GenotypeQuality
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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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Latino
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allele frequency: 7.352941176470588e-3
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East Asian
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European (Non-Finnish)
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African
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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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QD
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ClippingRankSum
type: SiteQuality
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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DP
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FS
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InbreedingCoeff
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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East Asian
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Latino
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Other
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African
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European (Non-Finnish)
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MQRankSum
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InbreedingCoeff
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QD
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DP
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VQSLOD
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FS
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BaseQRankSum
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MQ
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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European (Non-Finnish)
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Other
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European (Finnish)
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African
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East Asian
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BaseQRankSum
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ClippingRankSum
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QD
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MQRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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FS
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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South Asian
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East Asian
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Other
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European (Non-Finnish)
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African
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BaseQRankSum
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InbreedingCoeff
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DP
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MQ
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VQSLOD
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MQRankSum
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QD
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FS
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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East Asian
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Latino
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European (Finnish)
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Other
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European (Non-Finnish)
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MQRankSum
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DP
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QD
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MQ
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BaseQRankSum
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InbreedingCoeff
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FS
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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SIO_000300: 9.22e-1

GenotypeQuality
all individuals: 3109
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1172
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24788
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13934
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1990
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1580
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2639
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1331
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3088
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3001
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.458210422812193e-4
allele num: 4068
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12222
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2724
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1240
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1902
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1296
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 238
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.49477e5

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

QD
type: SiteQuality
SIO_000300: 5.4e0

MQ
type: SiteQuality
SIO_000300: 3.817e1

VQSLOD
type: SiteQuality
SIO_000300: -1.932e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.51e-2

GenotypeQuality
all individuals: 13934
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1172
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1990
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1331
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2639
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 90
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1902
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 238
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.458210422812193e-4
allele num: 4068
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12222
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1240
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2724
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1296
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.49477e5

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 3.817e1

VQSLOD
type: SiteQuality
SIO_000300: -1.932e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 5.4e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.51e-2

GenotypeQuality
all individuals: 157
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2994
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3056
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1246
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 851
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1364
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4314
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 258
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2008
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1428
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2840
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 7.583801001061732e-5
allele num: 13186
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.76908e5

VQSLOD
type: SiteQuality
SIO_000300: -4.815e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.8e-1

QD
type: SiteQuality
SIO_000300: 2.58e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.75e-1

FS
type: SiteQuality
SIO_000300: 1.827e0

MQRankSum
type: SiteQuality
SIO_000300: -4.281e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.24e0

MQ
type: SiteQuality
SIO_000300: 4.047e1

GenotypeQuality
all individuals: 359
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1561
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2663
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1963
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28101
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 885
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2959
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1191
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11759
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2999
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2639
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4348
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 260
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13350
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2864
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1386
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2028
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.5e0

MQ
type: SiteQuality
SIO_000300: 3.904e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.096e0

DP
type: SiteQuality
SIO_000300: 7.84148e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.36e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e0

QD
type: SiteQuality
SIO_000300: 1.089e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.495e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e0

GenotypeQuality
all individuals: 1091
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2765
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1103
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 482
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2707
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9904
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1294
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4395
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2643
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 99
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15070
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 286
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.137665669089354e-4
allele num: 4678
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1644
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3092
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2214
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1764
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.74e0

VQSLOD
type: SiteQuality
SIO_000300: -4.368e0

QD
type: SiteQuality
SIO_000300: 6.3e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.388e0

DP
type: SiteQuality
SIO_000300: 8.23359e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.001e0

MQ
type: SiteQuality
SIO_000300: 3.453e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-2

GenotypeQuality
all individuals: 6618
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2195
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2657
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

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

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 1.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2660
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3742
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5640
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20016
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2496
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 8.156606851549756e-4
allele num: 2452
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 332
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.919e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.42e-2

MQ
type: SiteQuality
SIO_000300: 3.904e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.689e0

DP
type: SiteQuality
SIO_000300: 9.17477e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.67e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.31e-1

QD
type: SiteQuality
SIO_000300: 1.766e1

GenotypeQuality
all individuals: 1879
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 173
bin: 5.25e1
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GenotypeQuality
all individuals: 436
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variant carriers: 1

GenotypeQuality
all individuals: 251
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variant carriers: 1

GenotypeQuality
all individuals: 31071
bin: 2.25e1
variant carriers: 2

GenotypeQuality
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bin: 4.25e1
variant carriers: 2

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 2.5e0
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 451
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variant carriers: 1

GenotypeQuality
all individuals: 201
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 88
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 281
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10808
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 115
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1136
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2720
bin: 9.75e1
variant carriers: 63

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2748
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2850
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 1.45032632342277e-3
allele num: 2758
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3960
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 57
allele frequency: 2.598942184935255e-3
allele num: 21932
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 3.355704697986577e-4
allele num: 5960
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 2.808988764044944e-3
allele num: 356
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.61e0

DP
type: SiteQuality
SIO_000300: 9.49459e5

QD
type: SiteQuality
SIO_000300: 1.279e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.37e-1

MQ
type: SiteQuality
SIO_000300: 4.128e1

FS
type: SiteQuality
SIO_000300: 5.896e0

MQRankSum
type: SiteQuality
SIO_000300: 7.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.8e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.604e0

GenotypeQuality
all individuals: 37189
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6759
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GenotypeQuality
all individuals: 3119
bin: 9.75e1
variant carriers: 2

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10230
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.424305722014861e-5
allele num: 58406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6444
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7802
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7178
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.683e0

DP
type: SiteQuality
SIO_000300: 1.500398e6

MQ
type: SiteQuality
SIO_000300: 4.056e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.174e0

QD
type: SiteQuality
SIO_000300: 3.64e0

GenotypeQuality
all individuals: 1315
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
all individuals: 94
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
all individuals: 1262
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.218323586744639e-4
allele num: 8208
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10652
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7544
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15674
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60410
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 4.317e1

MQRankSum
type: SiteQuality
SIO_000300: 1.7e-2

DP
type: SiteQuality
SIO_000300: 1.536476e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.872e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.06e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.277e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.17e-1

QD
type: SiteQuality
SIO_000300: 3.18e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
all individuals: 581
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GenotypeQuality
all individuals: 1392
bin: 7.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11018
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16120
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7852
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.832785617630002e-5
allele num: 62076
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -7.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.58e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.192e0

QD
type: SiteQuality
SIO_000300: 6.05e0

MQ
type: SiteQuality
SIO_000300: 4.393e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.27e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.56513e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.63e-1

GenotypeQuality
all individuals: 44
bin: 1.25e1
variant carriers: 21

GenotypeQuality
all individuals: 146
bin: 8.25e1
variant carriers: 111

GenotypeQuality
all individuals: 61
bin: 3.75e1
variant carriers: 40

GenotypeQuality
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variant carriers: 22

GenotypeQuality
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variant carriers: 18

GenotypeQuality
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variant carriers: 42

GenotypeQuality
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variant carriers: 24

GenotypeQuality
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bin: 1.75e1
variant carriers: 24

GenotypeQuality
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variant carriers: 50

GenotypeQuality
all individuals: 808
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variant carriers: 8

GenotypeQuality
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bin: 6.25e1
variant carriers: 94

GenotypeQuality
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bin: 5.25e1
variant carriers: 75

GenotypeQuality
all individuals: 143
bin: 9.25e1
variant carriers: 131

GenotypeQuality
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bin: 7.75e1
variant carriers: 107

GenotypeQuality
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bin: 7.25e1
variant carriers: 63

GenotypeQuality
all individuals: 311
bin: 6.75e1
variant carriers: 101

GenotypeQuality
all individuals: 54398
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variant carriers: 54294

GenotypeQuality
all individuals: 96
bin: 5.75e1
variant carriers: 72

GenotypeQuality
all individuals: 142
bin: 8.75e1
variant carriers: 123

Latino
type: Population
allele count: 5619
allele frequency: 4.966413293264981e-1
allele num: 11314
num of homozygotes: 52

East Asian
type: Population
allele count: 3338
allele frequency: 4.114891518737673e-1
allele num: 8112
num of homozygotes: 14

European (Non-Finnish)
type: Population
allele count: 31036
allele frequency: 4.892644323233597e-1
allele num: 63434
num of homozygotes: 89

Other
type: Population
allele count: 423
allele frequency: 4.839816933638444e-1
allele num: 874
num of homozygotes: 1

South Asian
type: Population
allele count: 7542
allele frequency: 4.630971386466904e-1
allele num: 16286
num of homozygotes: 21

European (Finnish)
type: Population
allele count: 3121
allele frequency: 4.754722730042657e-1
allele num: 6564
num of homozygotes: 3

African
type: Population
allele count: 4352
allele frequency: 4.718126626192541e-1
allele num: 9224
num of homozygotes: 16

QD
type: SiteQuality
SIO_000300: 1.069e1

MQ
type: SiteQuality
SIO_000300: 4.324e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.407e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.797e-1

FS
type: SiteQuality
SIO_000300: 1.059e0

MQRankSum
type: SiteQuality
SIO_000300: -2.05e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.868e0

VQSLOD
type: SiteQuality
SIO_000300: 1.4823e2

DP
type: SiteQuality
SIO_000300: 4.024073e6

GenotypeQuality
all individuals: 651
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 51171
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variant carriers: 1

GenotypeQuality
all individuals: 415
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variant carriers: 0

GenotypeQuality
all individuals: 58
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variant carriers: 0

GenotypeQuality
all individuals: 338
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GenotypeQuality
all individuals: 235
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variant carriers: 0

GenotypeQuality
all individuals: 113
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GenotypeQuality
all individuals: 172
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GenotypeQuality
all individuals: 469
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GenotypeQuality
all individuals: 726
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variant carriers: 0

GenotypeQuality
all individuals: 180
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GenotypeQuality
all individuals: 104
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variant carriers: 0

GenotypeQuality
all individuals: 366
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GenotypeQuality
all individuals: 294
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GenotypeQuality
all individuals: 77
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variant carriers: 0

GenotypeQuality
all individuals: 684
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GenotypeQuality
all individuals: 823
bin: 9.25e1
variant carriers: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.138952164009112e-3
allele num: 878
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8240
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9574
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11382
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64282
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.15e-1

QD
type: SiteQuality
SIO_000300: 8.210000000000001e0

DP
type: SiteQuality
SIO_000300: 4.133535e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.01e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.61e0

MQ
type: SiteQuality
SIO_000300: 4.155e1

VQSLOD
type: SiteQuality
SIO_000300: -2.204e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.05e0

GenotypeQuality
all individuals: 699
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variant carriers: 0

GenotypeQuality
all individuals: 78
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 113
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GenotypeQuality
all individuals: 465
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.778089887640449e-5
allele num: 11392
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16384
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64290
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8262
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9584
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

QD
type: SiteQuality
SIO_000300: 4.26e0

VQSLOD
type: SiteQuality
SIO_000300: -2.584e0

MQ
type: SiteQuality
SIO_000300: 4.367e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.78e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.12e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.636e0

DP
type: SiteQuality
SIO_000300: 4.13505e6

GenotypeQuality
all individuals: 370
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 51203
bin: 9.75e1
variant carriers: 10

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11420
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 1.036054703688355e-3
allele num: 9652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16436
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64464
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8312
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -2.346e0

VQSLOD
type: SiteQuality
SIO_000300: -2.926e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.022e0

FS
type: SiteQuality
SIO_000300: 2.21e0

DP
type: SiteQuality
SIO_000300: 4.144057e6

QD
type: SiteQuality
SIO_000300: 6.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 4.285e1

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

GenotypeQuality
all individuals: 26
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 840
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GenotypeQuality
all individuals: 51
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GenotypeQuality
all individuals: 481
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GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8324
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11420
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64486
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.034554107179805e-4
allele num: 9666
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 4.144862e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 9.119999999999999e0

FS
type: SiteQuality
SIO_000300: 3.082e0

VQSLOD
type: SiteQuality
SIO_000300: -3.547e0

MQ
type: SiteQuality
SIO_000300: 4.169e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.3e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.677e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.667e0

GenotypeQuality
all individuals: 50
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variant carriers: 0

GenotypeQuality
all individuals: 32
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GenotypeQuality
all individuals: 3578
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GenotypeQuality
all individuals: 44
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GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 282
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GenotypeQuality
all individuals: 21
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 854
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 482
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 51203
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 776
bin: 8.25e1
variant carriers: 0