1-57611012-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611012
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611012
    reference: chr 1
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.158C>T
  hgvsp: ENSP00000409328.2:p.Ser53Phe
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.158C>T
  hgvsp: ENSP00000360280.1:p.Ser53Phe
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.158C>T
  hgvsp: ENSP00000395296.2:p.Ser53Phe
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.158C>T
  hgvsp: ENSP00000360275.1:p.Ser53Phe
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.158C>T
  hgvsp: ENSP00000360274.1:p.Ser53Phe
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.158C>T
  hgvsp: ENSP00000360276.4:p.Ser53Phe
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.158C>T
  hgvsp: ENSP00000387581.2:p.Ser53Phe
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.158C>T
  hgvsp: ENSP00000360278.4:p.Ser53Phe
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.919C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.158C>T
  hgvsp: ENSP00000329120.6:p.Ser53Phe
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4340
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6406
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9147
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser53Phe
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP

1-57611024-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611024
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611024
    reference: chr 1
allele count: 1
allele frequency: 8.243887157672586e-6
allele num: 121302
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.146T>C
  hgvsp: ENSP00000360280.1:p.Ile49Thr
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.146T>C
  hgvsp: ENSP00000387581.2:p.Ile49Thr
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.146T>C
  hgvsp: ENSP00000395296.2:p.Ile49Thr
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.146T>C
  hgvsp: ENSP00000360276.4:p.Ile49Thr
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.146T>C
  hgvsp: ENSP00000329120.6:p.Ile49Thr
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.146T>C
  hgvsp: ENSP00000360278.4:p.Ile49Thr
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.146T>C
  hgvsp: ENSP00000409328.2:p.Ile49Thr
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.146T>C
  hgvsp: ENSP00000360274.1:p.Ile49Thr
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.907T>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.146T>C
  hgvsp: ENSP00000360275.1:p.Ile49Thr
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9141
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11433
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6405
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile49Thr
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

1-57611029-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611029
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611029
    reference: chr 1
allele count: 1
allele frequency: 8.243887157672586e-6
allele num: 121302
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.141C>T
  hgvsp: ENST00000371236.2:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.141C>T
  hgvsp: ENST00000420954.2:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.141C>T
  hgvsp: ENST00000414851.2:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.141C>T
  hgvsp: ENST00000371230.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.141C>T
  hgvsp: ENST00000439789.2:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.141C>T
  hgvsp: ENST00000371231.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.141C>T
  hgvsp: ENST00000371234.4:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.141C>T
  hgvsp: ENST00000371232.4:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.141C>T
  hgvsp: ENST00000332102.6:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.902C>T
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6404
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11434
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12267
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9127
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile47Ile
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

1-57611029-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611029
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611029
    reference: chr 1
allele count: 1
allele frequency: 8.243887157672586e-6
allele num: 121302
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.141C>A
  hgvsp: ENST00000439789.2:c.141C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.141C>A
  hgvsp: ENST00000420954.2:c.141C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.141C>A
  hgvsp: ENST00000414851.2:c.141C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.141C>A
  hgvsp: ENST00000371231.1:c.141C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.141C>A
  hgvsp: ENST00000371232.4:c.141C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.141C>A
  hgvsp: ENST00000332102.6:c.141C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.141C>A
  hgvsp: ENST00000371230.1:c.141C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.141C>A
  hgvsp: ENST00000371236.2:c.141C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.902C>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.141C>A
  hgvsp: ENST00000371234.4:c.141C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12267
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9127
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11434
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6404
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile47Ile
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP

1-57611034-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611034
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611034
    reference: chr 1
allele count: 4
allele frequency: 3.297228679295053e-5
allele num: 121314
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.136T>C
  hgvsp: ENST00000414851.2:c.136T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.136T>C
  hgvsp: ENST00000371230.1:c.136T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.136T>C
  hgvsp: ENST00000371236.2:c.136T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.136T>C
  hgvsp: ENST00000371234.4:c.136T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.136T>C
  hgvsp: ENST00000332102.6:c.136T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.136T>C
  hgvsp: ENST00000371231.1:c.136T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.897T>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.136T>C
  hgvsp: ENST00000439789.2:c.136T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.136T>C
  hgvsp: ENST00000420954.2:c.136T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.136T>C
  hgvsp: ENST00000371232.4:c.136T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11431
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4340
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu46Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

1-57611048-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611048
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611048
    reference: chr 1
allele count: 1
allele frequency: 8.24347940778844e-6
allele num: 121308
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.122G>A
  hgvsp: ENSP00000409328.2:p.Arg41Gln
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.122G>A
  hgvsp: ENSP00000395296.2:p.Arg41Gln
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.122G>A
  hgvsp: ENSP00000360276.4:p.Arg41Gln
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.122G>A
  hgvsp: ENSP00000387581.2:p.Arg41Gln
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.122G>A
  hgvsp: ENSP00000329120.6:p.Arg41Gln
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.122G>A
  hgvsp: ENSP00000360274.1:p.Arg41Gln
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.122G>A
  hgvsp: ENSP00000360280.1:p.Arg41Gln
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.122G>A
  hgvsp: ENSP00000360278.4:p.Arg41Gln
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.122G>A
  hgvsp: ENSP00000360275.1:p.Arg41Gln
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.883G>A
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9122
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12276
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg41Gln
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

1-57611052-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611052
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611052
    reference: chr 1
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.118G>A
  hgvsp: ENSP00000360280.1:p.Val40Ile
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.118G>A
  hgvsp: ENSP00000387581.2:p.Val40Ile
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.118G>A
  hgvsp: ENSP00000409328.2:p.Val40Ile
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.879G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.118G>A
  hgvsp: ENSP00000395296.2:p.Val40Ile
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.118G>A
  hgvsp: ENSP00000360278.4:p.Val40Ile
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.118G>A
  hgvsp: ENSP00000360276.4:p.Val40Ile
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.118G>A
  hgvsp: ENSP00000329120.6:p.Val40Ile
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.118G>A
  hgvsp: ENSP00000360274.1:p.Val40Ile
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.118G>A
  hgvsp: ENSP00000360275.1:p.Val40Ile
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11432
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12285
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9122
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val40Ile
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

1-57611061-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611061
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611061
    reference: chr 1
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.109G>A
  hgvsp: ENSP00000329120.6:p.Gly37Ser
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.109G>A
  hgvsp: ENSP00000409328.2:p.Gly37Ser
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.109G>A
  hgvsp: ENSP00000395296.2:p.Gly37Ser
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.109G>A
  hgvsp: ENSP00000360280.1:p.Gly37Ser
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.109G>A
  hgvsp: ENSP00000360276.4:p.Gly37Ser
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.109G>A
  hgvsp: ENSP00000360278.4:p.Gly37Ser
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.109G>A
  hgvsp: ENSP00000360274.1:p.Gly37Ser
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.109G>A
  hgvsp: ENSP00000360275.1:p.Gly37Ser
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.870G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.109G>A
  hgvsp: ENSP00000387581.2:p.Gly37Ser
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11438
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12292
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly37Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

1-57611062-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611062
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611062
    reference: chr 1
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.108A>G
  hgvsp: ENST00000439789.2:c.108A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.108A>G
  hgvsp: ENST00000371231.1:c.108A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.108A>G
  hgvsp: ENST00000371236.2:c.108A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.108A>G
  hgvsp: ENST00000332102.6:c.108A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.108A>G
  hgvsp: ENST00000420954.2:c.108A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.108A>G
  hgvsp: ENST00000414851.2:c.108A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.108A>G
  hgvsp: ENST00000371232.4:c.108A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.108A>G
  hgvsp: ENST00000371230.1:c.108A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.108A>G
  hgvsp: ENST00000371234.4:c.108A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.869A>G
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12291
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12735
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Lys36Lys
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

1-57611064-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611064
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611064
    reference: chr 1
allele count: 1
allele frequency: 8.242528148233626e-6
allele num: 121322
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.106A>G
  hgvsp: ENSP00000360274.1:p.Lys36Glu
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.106A>G
  hgvsp: ENSP00000395296.2:p.Lys36Glu
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.106A>G
  hgvsp: ENSP00000360275.1:p.Lys36Glu
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.106A>G
  hgvsp: ENSP00000360280.1:p.Lys36Glu
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.106A>G
  hgvsp: ENSP00000409328.2:p.Lys36Glu
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.106A>G
  hgvsp: ENSP00000360276.4:p.Lys36Glu
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.867A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.106A>G
  hgvsp: ENSP00000329120.6:p.Lys36Glu
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.106A>G
  hgvsp: ENSP00000360278.4:p.Lys36Glu
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.106A>G
  hgvsp: ENSP00000387581.2:p.Lys36Glu
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11438
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12294
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Lys36Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

1-57611071-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611071
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611071
    reference: chr 1
allele count: 3
allele frequency: 2.472799208704253e-5
allele num: 121320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.99G>A
  hgvsp: ENST00000414851.2:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.860G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.99G>A
  hgvsp: ENST00000371236.2:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.99G>A
  hgvsp: ENST00000371231.1:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.99G>A
  hgvsp: ENST00000420954.2:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.99G>A
  hgvsp: ENST00000371234.4:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.99G>A
  hgvsp: ENST00000371230.1:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.99G>A
  hgvsp: ENST00000439789.2:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.99G>A
  hgvsp: ENST00000332102.6:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.99G>A
  hgvsp: ENST00000371232.4:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2658
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Lys33Lys
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/1-57611071-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611071
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611071
    reference: chr 1
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.99G>T
  hgvsp: ENSP00000395296.2:p.Lys33Asn
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.99G>T
  hgvsp: ENSP00000329120.6:p.Lys33Asn
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.99G>T
  hgvsp: ENSP00000360274.1:p.Lys33Asn
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.99G>T
  hgvsp: ENSP00000360278.4:p.Lys33Asn
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.99G>T
  hgvsp: ENSP00000387581.2:p.Lys33Asn
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.99G>T
  hgvsp: ENSP00000409328.2:p.Lys33Asn
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.99G>T
  hgvsp: ENSP00000360275.1:p.Lys33Asn
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.99G>T
  hgvsp: ENSP00000360280.1:p.Lys33Asn
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.99G>T
  hgvsp: ENSP00000360276.4:p.Lys33Asn
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.860G>T
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2658
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12301
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Lys33Asn
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ

1-57611072-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611072
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611072
    reference: chr 1
allele count: 2
allele frequency: 1.648587160803192e-5
allele num: 121316
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.859A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.98A>G
  hgvsp: ENSP00000360280.1:p.Lys33Arg
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.98A>G
  hgvsp: ENSP00000329120.6:p.Lys33Arg
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.98A>G
  hgvsp: ENSP00000387581.2:p.Lys33Arg
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.98A>G
  hgvsp: ENSP00000360275.1:p.Lys33Arg
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.98A>G
  hgvsp: ENSP00000360278.4:p.Lys33Arg
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.98A>G
  hgvsp: ENSP00000360274.1:p.Lys33Arg
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.98A>G
  hgvsp: ENSP00000409328.2:p.Lys33Arg
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.98A>G
  hgvsp: ENSP00000360276.4:p.Lys33Arg
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.98A>G
  hgvsp: ENSP00000395296.2:p.Lys33Arg
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9090
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Lys33Arg
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

1-57611076-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611076
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611076
    reference: chr 1
allele count: 3
allele frequency: 2.472880741204788e-5
allele num: 121316
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.94A>C
  hgvsp: ENSP00000360280.1:p.Ile32Leu
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.94A>C
  hgvsp: ENSP00000360274.1:p.Ile32Leu
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.94A>C
  hgvsp: ENSP00000395296.2:p.Ile32Leu
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.94A>C
  hgvsp: ENSP00000329120.6:p.Ile32Leu
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.94A>C
  hgvsp: ENSP00000360276.4:p.Ile32Leu
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.94A>C
  hgvsp: ENSP00000409328.2:p.Ile32Leu
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.94A>C
  hgvsp: ENSP00000360278.4:p.Ile32Leu
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.94A>C
  hgvsp: ENSP00000387581.2:p.Ile32Leu
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.94A>C
  hgvsp: ENSP00000360275.1:p.Ile32Leu
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.855A>C
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12302
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8686
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11432
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile32Leu
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ

1-57611077-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611077
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611077
    reference: chr 1
allele count: 3
allele frequency: 2.472880741204788e-5
allele num: 121316
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.93G>A
  hgvsp: ENST00000439789.2:c.93G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.93G>A
  hgvsp: ENST00000414851.2:c.93G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.93G>A
  hgvsp: ENST00000371234.4:c.93G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.93G>A
  hgvsp: ENST00000332102.6:c.93G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.93G>A
  hgvsp: ENST00000371232.4:c.93G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.93G>A
  hgvsp: ENST00000371230.1:c.93G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.93G>A
  hgvsp: ENST00000420954.2:c.93G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.93G>A
  hgvsp: ENST00000371231.1:c.93G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.854G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.93G>A
  hgvsp: ENST00000371236.2:c.93G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11434
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9090
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8688
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3782
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu31Leu
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum

1-57611084-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611084
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611084
    reference: chr 1
allele count: 1
allele frequency: 8.242528148233626e-6
allele num: 121322
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.86C>T
  hgvsp: ENSP00000360278.4:p.Ala29Val
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.86C>T
  hgvsp: ENSP00000409328.2:p.Ala29Val
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.847C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.86C>T
  hgvsp: ENSP00000360280.1:p.Ala29Val
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.86C>T
  hgvsp: ENSP00000360276.4:p.Ala29Val
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.86C>T
  hgvsp: ENSP00000387581.2:p.Ala29Val
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.86C>T
  hgvsp: ENSP00000360275.1:p.Ala29Val
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.86C>T
  hgvsp: ENSP00000395296.2:p.Ala29Val
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.86C>T
  hgvsp: ENSP00000329120.6:p.Ala29Val
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.86C>T
  hgvsp: ENSP00000360274.1:p.Ala29Val
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9092
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8685
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11435
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala29Val
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

1-57611085-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611085
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611085
    reference: chr 1
allele count: 1
allele frequency: 8.242528148233626e-6
allele num: 121322
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.85G>A
  hgvsp: ENSP00000360275.1:p.Ala29Thr
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.85G>A
  hgvsp: ENSP00000360278.4:p.Ala29Thr
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.846G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.85G>A
  hgvsp: ENSP00000395296.2:p.Ala29Thr
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.85G>A
  hgvsp: ENSP00000409328.2:p.Ala29Thr
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.85G>A
  hgvsp: ENSP00000387581.2:p.Ala29Thr
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.85G>A
  hgvsp: ENSP00000360276.4:p.Ala29Thr
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.85G>A
  hgvsp: ENSP00000360280.1:p.Ala29Thr
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.85G>A
  hgvsp: ENSP00000360274.1:p.Ala29Thr
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.85G>A
  hgvsp: ENSP00000329120.6:p.Ala29Thr
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11435
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9094
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8685
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala29Thr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: African
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP

1-57611093-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611093
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611093
    reference: chr 1
allele count: 2
allele frequency: 1.648614339647526e-5
allele num: 121314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.77G>A
  hgvsp: ENSP00000395296.2:p.Arg26His
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.77G>A
  hgvsp: ENSP00000360274.1:p.Arg26His
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.77G>A
  hgvsp: ENSP00000360280.1:p.Arg26His
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.77G>A
  hgvsp: ENSP00000360276.4:p.Arg26His
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.77G>A
  hgvsp: ENSP00000387581.2:p.Arg26His
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.77G>A
  hgvsp: ENSP00000329120.6:p.Arg26His
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.838G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.77G>A
  hgvsp: ENSP00000360278.4:p.Arg26His
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.77G>A
  hgvsp: ENSP00000409328.2:p.Arg26His
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.77G>A
  hgvsp: ENSP00000360275.1:p.Arg26His
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.719G>A
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9086
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11428
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12297
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6404
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg26His
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

1-57611094-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611094
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611094
    reference: chr 1
allele count: 1
allele frequency: 8.243615319934711e-6
allele num: 121306
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.76C>G
  hgvsp: ENSP00000360276.4:p.Arg26Gly
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.76C>G
  hgvsp: ENSP00000329120.6:p.Arg26Gly
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.837C>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.76C>G
  hgvsp: ENSP00000360275.1:p.Arg26Gly
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.76C>G
  hgvsp: ENSP00000409328.2:p.Arg26Gly
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.76C>G
  hgvsp: ENSP00000360280.1:p.Arg26Gly
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.76C>G
  hgvsp: ENSP00000360278.4:p.Arg26Gly
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.718C>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.76C>G
  hgvsp: ENSP00000395296.2:p.Arg26Gly
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.76C>G
  hgvsp: ENSP00000387581.2:p.Arg26Gly
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.76C>G
  hgvsp: ENSP00000360274.1:p.Arg26Gly
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11427
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg26Gly
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

1-57611112-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611112
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611112
    reference: chr 1
allele count: 1
allele frequency: 8.247694769311978e-6
allele num: 121246
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.68-10C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.68-10C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.68-10C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.68-10C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.68-10C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.829-10C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.68-10C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.68-10C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.68-10C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.68-10C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.710-10C>T
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12263
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2658
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11406
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4342
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ

1-57611117-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611117
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611117
    reference: chr 1
allele count: 1
allele frequency: 8.249327679794096e-6
allele num: 121222
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.68-15T>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.68-15T>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.68-15T>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.829-15T>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.68-15T>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.68-15T>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.68-15T>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.710-15T>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.68-15T>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.68-15T>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.68-15T>C
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8972
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8675
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2658
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6398
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11391
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5807
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

1-57611121-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611121
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611121
    reference: chr 1
allele count: 2
allele frequency: 1.65000165000165e-5
allele num: 121212
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.68-19C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.68-19C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.710-19C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.68-19C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.68-19C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.68-19C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.829-19C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.68-19C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.68-19C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.68-19C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.68-19C>T
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12187
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8675
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4342
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11369
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8929
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2658
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6398
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

1-57611124-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611124
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611123
    reference: chr 1
allele count: 1
allele frequency: 8.25082508250825e-6
allele num: 121200
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.68-23delG
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.68-23delG
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.68-23delG
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.68-23delG
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.710-23delG
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.68-23delG
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.829-23delG
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.68-23delG
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.68-23delG
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.68-23delG
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.68-23delG
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6395
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12123
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8887
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8669
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: TC
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP

1-57611127-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611127
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611127
    reference: chr 1
allele count: 2
allele frequency: 1.650355651642929e-5
allele num: 121186
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.68-25T>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.710-25T>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.68-25T>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.68-25T>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.68-25T>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.68-25T>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.68-25T>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.68-25T>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.68-25T>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.68-25T>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.829-25T>A
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12063
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6395
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8823
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11301
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD

1-57611128-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611128
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611128
    reference: chr 1
allele count: 1
allele frequency: 8.252323028932645e-6
allele num: 121178
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.68-26T>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.68-26T>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.68-26T>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.68-26T>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.68-26T>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.829-26T>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.710-26T>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.68-26T>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.68-26T>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.68-26T>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.68-26T>A
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4342
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11290
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12017
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8662
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

1-57611129-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611129
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611129
    reference: chr 1
allele count: 1
allele frequency: 8.253276550790664e-6
allele num: 121164
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.68-27A>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.68-27A>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.68-27A>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.68-27A>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.68-27A>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.68-27A>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.68-27A>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.68-27A>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.710-27A>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.829-27A>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.68-27A>T
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11966
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8754
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8662
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11269
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4342
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum

1-57611139-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611139
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611139
    reference: chr 1
allele count: 2
allele frequency: 1.651418568550385e-5
allele num: 121108
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.710-37A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.68-37A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.68-37A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.68-37A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.68-37A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.829-37A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.68-37A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.68-37A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.68-37A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.68-37A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.68-37A>G
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11555
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8639
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

1-57611143-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611143
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611143
    reference: chr 1
allele count: 1
allele frequency: 8.261595148791329e-6
allele num: 121042
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.710-41C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.68-41C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.68-41C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.68-41C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.68-41C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.68-41C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.68-41C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.68-41C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.68-41C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.829-41C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.68-41C>T
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10967
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8615
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11242
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8441
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6379
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 2.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/1-57611145-CCCCA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611145
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611141
    reference: chr 1
allele count: 1
allele frequency: 8.261595148791329e-6
allele num: 121042
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.68-47_68-44delTGGG
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.68-47_68-44delTGGG
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.68-47_68-44delTGGG
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.68-47_68-44delTGGG
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.68-47_68-44delTGGG
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.68-47_68-44delTGGG
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.68-47_68-44delTGGG
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.710-47_710-44delTGGG
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.68-47_68-44delTGGG
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.829-47_829-44delTGGG
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.68-47_68-44delTGGG
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8452
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8642
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11240
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10954
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: East Asian
reference allele: CCCCA
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

1-57611146-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611146
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611146
    reference: chr 1
allele count: 1
allele frequency: 8.263779852904718e-6
allele num: 121010
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.68-44G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.68-44G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.68-44G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.68-44G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.68-44G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.68-44G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.710-44G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.829-44G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.68-44G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.68-44G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.68-44G>A
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8522
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4340
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6373
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3001
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

1-57611147-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611147
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611147
    reference: chr 1
allele count: 3
allele frequency: 2.479830710223515e-5
allele num: 120976
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.68-45G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.68-45G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.829-45G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.68-45G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.68-45G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.68-45G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.68-45G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.68-45G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.68-45G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.68-45G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.710-45G>A
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8619
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10931
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11120
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8600
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6372
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2661
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

http://identifiers.org/exac.variant/1-57611147-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611147
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611147
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 120976
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.68-45G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.68-45G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.68-45G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.68-45G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.68-45G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.68-45G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.68-45G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.710-45G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.68-45G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.68-45G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.829-45G>T
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11120
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8619
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10931
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8600
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6372
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

1-57611150-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611150
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611150
    reference: chr 1
allele count: 3
allele frequency: 2.481225394514838e-5
allele num: 120908
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.68-48C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.68-48C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.710-48C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.68-48C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.68-48C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.68-48C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.68-48C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.68-48C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.68-48C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.68-48C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.829-48C>T
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10785
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8599
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6351
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11036
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2661
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-57611151-TGGC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57611151
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57611148
    reference: chr 1
allele count: 1
allele frequency: 8.271709100534353e-6
allele num: 120894
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.68-52_68-50delGCC
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.829-52_829-50delGCC
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.68-52_68-50delGCC
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.68-52_68-50delGCC
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.710-52_710-50delGCC
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.68-52_68-50delGCC
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.68-52_68-50delGCC
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.68-52_68-50delGCC
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.68-52_68-50delGCC
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.68-52_68-50delGCC
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.68-52_68-50delGCC
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10760
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8593
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8862
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2399
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: TGGC
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-57756589-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57756589
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57756589
    reference: chr 1
allele count: 2
allele frequency: 1.674228599172931e-5
allele num: 119458
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.67+47G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.67+47G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.67+47G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.67+47G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.709+47G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.67+47G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.67+47G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.67+47G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.67+47G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.828+47G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.67+47G>A
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4294
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11044
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12332
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3984
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7290
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6908
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD

1-57756590-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57756590
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57756590
    reference: chr 1
allele count: 1
allele frequency: 8.369321415419637e-6
allele num: 119484
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.67+46G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.67+46G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.67+46G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.67+46G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.709+46G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.67+46G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.67+46G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.67+46G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.67+46G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.67+46G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.828+46G>A
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7299
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9754
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12385
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2428
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11079
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1020
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-57756597-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57756597
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57756597
    reference: chr 1
allele count: 1
allele frequency: 8.352683717278361e-6
allele num: 119722
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.67+39C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.709+39C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.67+39C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.67+39C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.67+39C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.67+39C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.828+39C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.67+39C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.67+39C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.67+39C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.67+39C>T
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7318
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11434
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11415
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12799
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

1-57756597-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57756597
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57756596
    reference: chr 1
allele count: 6
allele frequency: 5.011610230367017e-5
allele num: 119722
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.67+38delT
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.67+38delT
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.67+38delT
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.67+38delT
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.67+38delT
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.67+38delT
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.67+38delT
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.67+38delT
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.709+38delT
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.67+38delT
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.828+38delT
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11415
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11434
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4308
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7318
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 15677
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: GA
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP

1-57756602-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57756602
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57756602
    reference: chr 1
allele count: 23
allele frequency: 1.922883991572752e-4
allele num: 119612
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.67+34C>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.67+34C>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.67+34C>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.67+34C>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.67+34C>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.828+34C>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.67+34C>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.67+34C>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.709+34C>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.67+34C>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.67+34C>A
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7325
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11514
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13051
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 9.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.25e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-57756605-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57756605
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57756605
    reference: chr 1
allele count: 1
allele frequency: 8.334583520861462e-6
allele num: 119982
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.67+31C>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.67+31C>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.67+31C>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.67+31C>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.67+31C>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.709+31C>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.828+31C>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.67+31C>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.67+31C>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.67+31C>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.67+31C>A
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7365
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11617
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4318
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13312
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 716
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

1-57756606-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57756606
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57756606
    reference: chr 1
allele count: 1
allele frequency: 8.333750020834376e-6
allele num: 119994
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.67+30G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.709+30G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.67+30G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.67+30G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.67+30G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.67+30G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.67+30G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.67+30G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.67+30G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.67+30G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.828+30G>A
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13412
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4323
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12671
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11665
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ

1-57756610-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57756610
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57756610
    reference: chr 1
allele count: 2
allele frequency: 1.666139055965611e-5
allele num: 120038
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.67+26A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.67+26A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.67+26A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.67+26A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.828+26A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.67+26A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.67+26A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.67+26A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.67+26A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.709+26A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.67+26A>G
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12656
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7398
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11848
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2351
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4362
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD

1-57756610-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57756610
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57756609
    reference: chr 1
allele count: 1
allele frequency: 8.330695279828055e-6
allele num: 120038
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.67+25delT
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.67+25delT
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.67+25delT
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.67+25delT
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.67+25delT
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.67+25delT
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.828+25delT
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.67+25delT
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.67+25delT
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.709+25delT
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.67+25delT
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12656
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7398
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11848
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2328
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: TA
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

1-57756628-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57756628
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57756628
    reference: chr 1
allele count: 7
allele frequency: 5.794414184725924e-5
allele num: 120806
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.67+8T>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.67+8T>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.67+8T>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.67+8T>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.67+8T>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.67+8T>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.67+8T>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.828+8T>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.67+8T>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.67+8T>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.709+8T>C
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14353
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7390
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4326
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.67+8T>C
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

1-57756630-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57756630
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57756630
    reference: chr 1
allele count: 2
allele frequency: 1.655163281857755e-5
allele num: 120834
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.828+6G>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.67+6G>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.67+6G>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.67+6G>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.67+6G>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.67+6G>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.67+6G>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.67+6G>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.67+6G>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.67+6G>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.709+6G>C
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14380
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7397
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13237
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11932
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.67+6G>C
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

1-57756630-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57756630
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57756630
    reference: chr 1
allele count: 1
allele frequency: 8.275816409288777e-6
allele num: 120834
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.67+6G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.67+6G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.67+6G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.67+6G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.67+6G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.67+6G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.67+6G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.828+6G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.67+6G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.67+6G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.709+6G>A
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13237
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14380
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11932
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.67+6G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

1-57756638-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57756638
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57756638
    reference: chr 1
allele count: 1
allele frequency: 8.266375690242371e-6
allele num: 120972
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.65A>T
  hgvsp: ENSP00000360274.1:p.Lys22Ile
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.65A>T
  hgvsp: ENSP00000360275.1:p.Lys22Ile
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.65A>T
  hgvsp: ENSP00000387581.2:p.Lys22Ile
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.826A>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.65A>T
  hgvsp: ENSP00000329120.6:p.Lys22Ile
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.707A>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.65A>T
  hgvsp: ENSP00000360280.1:p.Lys22Ile
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.65A>T
  hgvsp: ENSP00000409328.2:p.Lys22Ile
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.65A>T
  hgvsp: ENSP00000395296.2:p.Lys22Ile
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.65A>T
  hgvsp: ENSP00000360278.4:p.Lys22Ile
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.65A>T
  hgvsp: ENSP00000360276.4:p.Lys22Ile
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14460
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11947
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13274
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys22Ile
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

1-57756646-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57756646
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57756646
    reference: chr 1
allele count: 1
allele frequency: 8.260776182530111e-6
allele num: 121054
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.57C>G
  hgvsp: ENST00000371234.4:c.57C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.57C>G
  hgvsp: ENST00000414851.2:c.57C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.57C>G
  hgvsp: ENST00000439789.2:c.57C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.57C>G
  hgvsp: ENST00000371231.1:c.57C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.57C>G
  hgvsp: ENST00000371230.1:c.57C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.699C>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.57C>G
  hgvsp: ENST00000420954.2:c.57C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.57C>G
  hgvsp: ENST00000332102.6:c.57C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.57C>G
  hgvsp: ENST00000371232.4:c.57C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.57C>G
  hgvsp: ENST00000371236.2:c.57C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.818C>G
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11954
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13311
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4327
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser19Ser
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

1-57756660-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57756660
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57756660
    reference: chr 1
allele count: 11
allele frequency: 9.081752282822278e-5
allele num: 121122
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.804G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.43G>A
  hgvsp: ENSP00000360274.1:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.43G>A
  hgvsp: ENSP00000387581.2:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.43G>A
  hgvsp: ENSP00000360280.1:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.43G>A
  hgvsp: ENSP00000360276.4:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.43G>A
  hgvsp: ENSP00000360275.1:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.43G>A
  hgvsp: ENSP00000409328.2:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.43G>A
  hgvsp: ENSP00000395296.2:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.685G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.43G>A
  hgvsp: ENSP00000329120.6:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.43G>A
  hgvsp: ENSP00000360278.4:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11966
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7386
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14519
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala15Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ

1-57756661-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57756661
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57756661
    reference: chr 1
allele count: 1
allele frequency: 8.255320554097116e-6
allele num: 121134
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.42C>T
  hgvsp: ENST00000371236.2:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.803C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.684C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.42C>T
  hgvsp: ENST00000371232.4:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.42C>T
  hgvsp: ENST00000420954.2:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.42C>T
  hgvsp: ENST00000371231.1:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.42C>T
  hgvsp: ENST00000332102.6:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.42C>T
  hgvsp: ENST00000371230.1:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.42C>T
  hgvsp: ENST00000439789.2:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.42C>T
  hgvsp: ENST00000414851.2:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.42C>T
  hgvsp: ENST00000371234.4:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11966
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13319
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14532
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7386
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser14Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

1-57756679-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57756679
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57756679
    reference: chr 1
allele count: 1
allele frequency: 8.254366559910193e-6
allele num: 121148
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.24A>G
  hgvsp: ENST00000420954.2:c.24A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.666A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.24A>G
  hgvsp: ENST00000371231.1:c.24A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.24A>G
  hgvsp: ENST00000439789.2:c.24A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.24A>G
  hgvsp: ENST00000371234.4:c.24A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.24A>G
  hgvsp: ENST00000332102.6:c.24A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.24A>G
  hgvsp: ENST00000371232.4:c.24A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.24A>G
  hgvsp: ENST00000371236.2:c.24A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.24A>G
  hgvsp: ENST00000414851.2:c.24A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.24A>G
  hgvsp: ENST00000371230.1:c.24A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.785A>G
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7383
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11961
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13302
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln8Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/1-57756707-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57756707
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57756707
    reference: chr 1
allele count: 1
allele frequency: 8.261458643138033e-6
allele num: 121044
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.-5G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.-5G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.638G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.-5G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.-5G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.-5G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.-5G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.-5G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.-5G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.-5G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.757G>T
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11963
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7386
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14527
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

1-57756708-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57756708
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57756708
    reference: chr 1
allele count: 1
allele frequency: 8.261322141995606e-6
allele num: 121046
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.-6A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.756A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.-6A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.-6A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.-6A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.-6A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.-6A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.-6A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.637A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.-6A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.-6A>G
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11959
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14530
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7388
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/1-57756714-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57756714
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57756714
    reference: chr 1
allele count: 4
allele frequency: 3.306768956053041e-5
allele num: 120964
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.-12G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.-12G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.-12G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.-12G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.-12G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.631G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.-12G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.-12G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.-12G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.-12G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.750G>T
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7385
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4285
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD

1-57756718-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57756718
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57756718
    reference: chr 1
allele count: 10
allele frequency: 8.267605866693124e-5
allele num: 120954
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.-16C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.627C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.-16C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.-16C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.-16C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.-16C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.-16C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.-16C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.-16C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.746C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.-16C>T
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4325
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7388
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12639
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11946
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

1-57756737-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57756737
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57756737
    reference: chr 1
allele count: 1
allele frequency: 8.29531314807134e-6
allele num: 120550
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.-35G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.608G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.-35G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.-35G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000329120
  ensembl transcript: ENST00000332102
  gene symbol: DAB1
  hgvsc: ENST00000332102.6:c.-35G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.727G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.-35G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360276
  ensembl transcript: ENST00000371232
  gene symbol: DAB1
  hgvsc: ENST00000371232.4:c.-35G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.-35G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360275
  ensembl transcript: ENST00000371231
  gene symbol: DAB1
  hgvsc: ENST00000371231.1:c.-35G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.-35G>A
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7373
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13624
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

1-57756738-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57756738
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57756738
    reference: chr 1
allele count: 26
allele frequency: 2.156709856164043e-4
allele num: 120554
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.-36C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.-36C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.607C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.-36C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.-36C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.-36C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.726C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.-36C>T
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7364
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13684
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10255
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4316
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11770
  bin: 3.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 7179
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15488
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1026
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14587
  bin: 9.75e1
  variant carriers: 26
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

1-57756738-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57756738
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57756738
    reference: chr 1
allele count: 1
allele frequency: 8.295037908323241e-6
allele num: 120554
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.-36C>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.726C>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.-36C>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.-36C>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.-36C>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.-36C>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.-36C>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.607C>G
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4316
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11770
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3497
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1004
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1026
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 981
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-57756738-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57756738
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57756738
    reference: chr 1
allele count: 2
allele frequency: 1.659007581664648e-5
allele num: 120554
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000395296
  ensembl transcript: ENST00000420954
  gene symbol: DAB1
  hgvsc: ENST00000420954.2:c.-36C>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000387581
  ensembl transcript: ENST00000414851
  gene symbol: DAB1
  hgvsc: ENST00000414851.2:c.-36C>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.726C>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000409328
  ensembl transcript: ENST00000439789
  gene symbol: DAB1
  hgvsc: ENST00000439789.2:c.-36C>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.-36C>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.-36C>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.607C>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.-36C>A
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4316
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11770
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5033
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2321
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1004
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15488
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

1-57756744-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57756744
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57756744
    reference: chr 1
allele count: 3
allele frequency: 2.492481015602931e-5
allele num: 120362
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.720G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.-42G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.-42G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.-42G>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.601G>A
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7319
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12914
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11556
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9953
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1075
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1556
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6696
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14568
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1223
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 748
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3171
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3423
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1314
  bin: 3.25e1
  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: C
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ

1-57756745-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57756745
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57756745
    reference: chr 1
allele count: 5
allele frequency: 4.154411153763065e-5
allele num: 120354
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.-43C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.719C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.-43C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.-43C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.600C>T
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7318
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11496
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12963
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3710
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9955
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4314
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3409
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1323
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4974
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1221
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13418
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6674
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 861
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4228
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1564
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

1-57756746-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57756746
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 57756746
    reference: chr 1
allele count: 4
allele frequency: 3.325407778128793e-5
allele num: 120286
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000473821
  gene symbol: DAB1
  hgvsc: ENST00000473821.1:n.599C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.-44C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360280
  ensembl transcript: ENST00000371236
  gene symbol: DAB1
  hgvsc: ENST00000371236.2:c.-44C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360274
  ensembl transcript: ENST00000371230
  gene symbol: DAB1
  hgvsc: ENST00000371230.1:c.-44C>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.718C>T
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7327
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11454
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12812
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10126
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3705
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13012
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6616
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1342
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1630
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
  all individuals: 689
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1401
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3169
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14563
  bin: 9.75e1
  variant carriers: 4
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

1-58521756-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58521756
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 58521756
    reference: chr 1
allele count: 343
allele frequency: 3.754378283712784e-2
allele num: 9136
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.387+94427T>A
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.-374-171922T>A
  variant of: http://identifiers.org/hgnc/2661
canonical: false
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 4.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 3.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 8409
  bin: 1.25e1
  variant carriers: 133
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 1.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 24068
  bin: 7.5e0
  variant carriers: 152
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 3.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 14380
  bin: 2.5e0
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 2.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3345
  bin: 1.75e1
  variant carriers: 28
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 5.75e1
  variant carriers: 34
genotype quality: GenotypeQuality
  all individuals: 747
  bin: 2.75e1
  variant carriers: 56
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 50
genotype quality: GenotypeQuality
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  bin: 9.75e1
  variant carriers: 41
genotype quality: GenotypeQuality
  all individuals: 28482
  bin: 2.5e0
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 4.75e1
  variant carriers: 43
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 3.25e1
  variant carriers: 37
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 4.25e1
  variant carriers: 46
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 7.75e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 11215
  bin: 7.5e0
  variant carriers: 51
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 7.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 3988
  bin: 1.25e1
  variant carriers: 40
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 5.25e1
  variant carriers: 25
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 9.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 41
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genotype quality: GenotypeQuality
  all individuals: 409
  bin: 3.75e1
  variant carriers: 43
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 6.25e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 8.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 6.75e1
  variant carriers: 17
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 23
  allele frequency: 7.516339869281045e-2
  allele num: 306
  num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

1-58521772-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58521772
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 58521772
    reference: chr 1
allele count: 32
allele frequency: 1.689902830587241e-3
allele num: 18936
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.-374-171938A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.387+94411A>G
  variant of: http://identifiers.org/hgnc/2661
canonical: false
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 22228
  bin: 7.5e0
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 84
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21483
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 5.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 3591
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  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 951
  bin: 3.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 4.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 201
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7974
  bin: 2.5e0
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 910
  bin: 9.75e1
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genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 10102
  bin: 2.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 4988
  bin: 1.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 308
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genotype quality: GenotypeQuality
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  bin: 8.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 80
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  variant carriers: 0
num of homozygotes: 0
population: African
  type: Population
  allele count: 5
  allele frequency: 4.970178926441352e-3
  allele num: 1006
  num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

1-58521794-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58521794
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 58521794
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 32988
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.-374-171960T>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.387+94389T>C
  variant of: http://identifiers.org/hgnc/2661
canonical: false
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
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genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1483
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 600
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 15244
  num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff

1-58521799-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58521799
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 58521799
    reference: chr 1
allele count: 1
allele frequency: 2.4997500249975e-5
allele num: 40004
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.387+94384T>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.-374-171965T>C
  variant of: http://identifiers.org/hgnc/2661
canonical: false
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 8839
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3016
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34421
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6867
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3023
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1492
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9085
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 702
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1124
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36625
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 955
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2094
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2960
  num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/1-58521808-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58521808
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 58521808
    reference: chr 1
allele count: 1
allele frequency: 1.532707988474036e-5
allele num: 65244
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223416
  ensembl transcript: ENST00000488067
  gene symbol: RPS26P15
  hgvsc: ENST00000488067.1:n.345G>T
  variant of: http://identifiers.org/hgnc/35680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.387+94375G>T
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.-374-171974G>T
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4022
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23421
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 1.75e1
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genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1134
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24202
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22692
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1371
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 962
  bin: 9.75e1
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genotype quality: GenotypeQuality
  all individuals: 791
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

1-58521810-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58521810
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 58521810
    reference: chr 1
allele count: 1
allele frequency: 1.423284941645317e-5
allele num: 70260
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223416
  ensembl transcript: ENST00000488067
  gene symbol: RPS26P15
  hgvsc: ENST00000488067.1:n.343A>G
  variant of: http://identifiers.org/hgnc/35680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.387+94373A>G
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.-374-171976A>G
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21094
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3546
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25520
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1238
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 962
  bin: 9.75e1
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genotype quality: GenotypeQuality
  all individuals: 512
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 1069
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 24766
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 737
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 246
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

1-58521817-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58521817
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 58521817
    reference: chr 1
allele count: 1
allele frequency: 1.179356543070101e-5
allele num: 84792
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl protein: ENSP00000360278
  ensembl transcript: ENST00000371234
  gene symbol: DAB1
  hgvsc: ENST00000371234.4:c.-374-171983A>C
  variant of: http://identifiers.org/hgnc/2661
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223416
  ensembl transcript: ENST00000488067
  gene symbol: RPS26P15
  hgvsc: ENST00000488067.1:n.336A>C
  variant of: http://identifiers.org/hgnc/35680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173406
  ensembl transcript: ENST00000485760
  gene symbol: DAB1
  hgvsc: ENST00000485760.1:n.387+94366A>C
  variant of: http://identifiers.org/hgnc/2661
canonical: true
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3573
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 1.75e1
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genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
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genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33060
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2459
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1214
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
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  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 615
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff

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

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

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

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

GenotypeQuality
all individuals: 4332
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 12728
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3785
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3086
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4589
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5856
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23801
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2409
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

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

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.166044776119403e-4
allele num: 8576
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

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

BaseQRankSum
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SIO_000300: -4.443e0

QD
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MQRankSum
type: SiteQuality
SIO_000300: -5.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.5e0

VQSLOD
type: SiteQuality
SIO_000300: -1.86e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.71e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.87e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.207e0

DP
type: SiteQuality
SIO_000300: 2.245376e6

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

BaseQRankSum
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SIO_000300: 2.83e0

MQRankSum
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SIO_000300: -4.04e-1

FS
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SIO_000300: 5.971e0

MQ
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SIO_000300: 6.0e1

VQSLOD
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SIO_000300: 6.12e-1

InbreedingCoeff
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SIO_000300: 1.39e-2

ClippingRankSum
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SIO_000300: 2.59e-1

DP
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SIO_000300: 2.245632e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.9e-2

QD
type: SiteQuality
SIO_000300: 1.367e1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66716
num of homozygotes: 0

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

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

South Asian
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allele frequency: 0.0e0
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InbreedingCoeff
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SIO_000300: 8.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: 8.0e-3

MQ
type: SiteQuality
SIO_000300: 5.95e1

BaseQRankSum
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SIO_000300: 9.68e-1

QD
type: SiteQuality
SIO_000300: 1.164e1

VQSLOD
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SIO_000300: 2.82e0

DP
type: SiteQuality
SIO_000300: 2.245704e6

MQRankSum
type: SiteQuality
SIO_000300: 5.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.99e-1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66716
num of homozygotes: 0

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
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SIO_000300: 5.69e-1

MQ
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SIO_000300: 5.95e1

QD
type: SiteQuality
SIO_000300: 1.164e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.0e-3

BaseQRankSum
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SIO_000300: 9.68e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.82e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.99e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

DP
type: SiteQuality
SIO_000300: 2.245704e6

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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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 4

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.165772907437631e-4
allele num: 8578
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727712508638562e-4
allele num: 11576
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.725e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

ClippingRankSum
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QD
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MQRankSum
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BaseQRankSum
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DP
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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GenotypeQuality
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variant carriers: 1

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

Other
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South Asian
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BaseQRankSum
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SIO_000300: 1.42e0

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

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

African
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num of homozygotes: 0

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

Latino
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num of homozygotes: 0

East Asian
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South Asian
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allele frequency: 6.056935190793458e-5
allele num: 16510
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European (Non-Finnish)
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allele count: 0
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QD
type: SiteQuality
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InbreedingCoeff
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MQ
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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FS
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VQSLOD
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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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variant carriers: 0

South Asian
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.25e-1

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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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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BaseQRankSum
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DP
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GenotypeQuality
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variant carriers: 0

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

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

African
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allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

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

Other
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
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FS
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MQRankSum
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ReadPosRankSum
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VQSLOD
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QD
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.246066e6

MQ
type: SiteQuality
SIO_000300: 5.896e1

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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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

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

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

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

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

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

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

MQ
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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FS
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BaseQRankSum
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QD
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SIO_000300: 8.640000000000001e0

ClippingRankSum
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SIO_000300: -1.784e0

DP
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SIO_000300: 2.246107e6

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.495459585818323e-5
allele num: 66734
num of homozygotes: 0

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

VQSLOD
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FS
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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QD
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ClippingRankSum
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MQ
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MQRankSum
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DP
type: SiteQuality
SIO_000300: 2.246344e6

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

BaseQRankSum
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SIO_000300: -1.612e0

QD
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InbreedingCoeff
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SIO_000300: 1.0e-4

ClippingRankSum
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ReadPosRankSum
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VQSLOD
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MQRankSum
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FS
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DP
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MQ
type: SiteQuality
SIO_000300: 5.984e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

South Asian
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allele count: 2
allele frequency: 1.211387038158692e-4
allele num: 16510
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

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

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

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

South Asian
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allele frequency: 1.817300702689605e-4
allele num: 16508
num of homozygotes: 0

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

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

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

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

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

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

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

Latino
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allele count: 0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 3
allele frequency: 4.495594317568783e-5
allele num: 66732
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
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

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

Latino
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allele frequency: 0.0e0
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African
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allele frequency: 9.609840476648087e-5
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -2.0e-4

BaseQRankSum
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ReadPosRankSum
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QD
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DP
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SIO_000300: 2.246081e6

VQSLOD
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SIO_000300: 8.65e-1

FS
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SIO_000300: 3.876e0

ClippingRankSum
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SIO_000300: 4.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.61e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

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

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

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

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

African
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allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.946e1

VQSLOD
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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QD
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SIO_000300: 1.526e1

FS
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SIO_000300: 5.151e0

ReadPosRankSum
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SIO_000300: -8.4e-1

DP
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SIO_000300: 2.246104e6

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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South Asian
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allele num: 16508
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QD
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MQRankSum
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VQSLOD
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BaseQRankSum
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MQ
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ClippingRankSum
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FS
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InbreedingCoeff
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SIO_000300: -1.0e-4

DP
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SIO_000300: 2.245907e6

ReadPosRankSum
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GenotypeDepth
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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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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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num of homozygotes: 0

InbreedingCoeff
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QD
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ReadPosRankSum
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FS
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VQSLOD
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DP
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SIO_000300: 2.245835e6

MQ
type: SiteQuality
SIO_000300: 5.962e1

BaseQRankSum
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SIO_000300: 9.68e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.94e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
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allele num: 66696
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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East Asian
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Other
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DP
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InbreedingCoeff
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FS
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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QD
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VQSLOD
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MQ
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GenotypeQuality
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variant carriers: 0

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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FS
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QD
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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DP
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BaseQRankSum
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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African
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European (Non-Finnish)
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allele frequency: 2.999220202747286e-5
allele num: 66684
num of homozygotes: 0

Other
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DP
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InbreedingCoeff
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ReadPosRankSum
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FS
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MQRankSum
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QD
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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African
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Other
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European (Non-Finnish)
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allele count: 1
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allele num: 66682
num of homozygotes: 0

Latino
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num of homozygotes: 0

South Asian
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FS
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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MQRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.336448598130841e-4
allele num: 8560
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66680
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.39e-1

DP
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SIO_000300: 2.237513e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.02e-1

BaseQRankSum
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SIO_000300: -1.727e0

MQ
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SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

QD
type: SiteQuality
SIO_000300: 1.219e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499745043342632e-5
allele num: 66678
num of homozygotes: 0

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -9.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.84e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

QD
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SIO_000300: 1.134e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.92e0

DP
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SIO_000300: 2.236511e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.4e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.73e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

GenotypeQuality
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variant carriers: 0

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

African
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allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499925003749813e-5
allele num: 66670
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
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SIO_000300: 6.43e-1

ClippingRankSum
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SIO_000300: 6.1e-2

InbreedingCoeff
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DP
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ReadPosRankSum
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SIO_000300: -6.33e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.108e-1

FS
type: SiteQuality
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MQ
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SIO_000300: 6.018e1

QD
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SIO_000300: 1.429e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.0e0

GenotypeQuality
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variant carriers: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.00048007681229e-5
allele num: 66656
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.1059e1

VQSLOD
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ReadPosRankSum
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SIO_000300: -1.082e0

MQ
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BaseQRankSum
type: SiteQuality
SIO_000300: -9.07e-1

QD
type: SiteQuality
SIO_000300: 1.035e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e0

MQRankSum
type: SiteQuality
SIO_000300: 3.02e-1

DP
type: SiteQuality
SIO_000300: 2.225609e6

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10310
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500915558490679e-5
allele num: 66626
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.419e0

InbreedingCoeff
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SIO_000300: 2.4e-3

QD
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MQ
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ClippingRankSum
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FS
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MQRankSum
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VQSLOD
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BaseQRankSum
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SIO_000300: -1.826e0

DP
type: SiteQuality
SIO_000300: 2.219352e6

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele 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: 908
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.883e0

ReadPosRankSum
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QD
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MQRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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VQSLOD
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MQ
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DP
type: SiteQuality
SIO_000300: 2.219113e6

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

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

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

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

European (Non-Finnish)
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allele frequency: 1.501231009427731e-5
allele num: 66612
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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QD
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InbreedingCoeff
type: SiteQuality
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VQSLOD
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BaseQRankSum
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FS
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DP
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MQRankSum
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.504775061565259e-5
allele num: 66596
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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MQRankSum
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SIO_000300: 2.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.691e0

VQSLOD
type: SiteQuality
SIO_000300: -2.694e-1

MQ
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SIO_000300: 5.89e1

QD
type: SiteQuality
SIO_000300: 1.039e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

DP
type: SiteQuality
SIO_000300: 2.217893e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.73e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.67e-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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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66596
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10288
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.691e0

FS
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ClippingRankSum
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SIO_000300: 6.67e-1

QD
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InbreedingCoeff
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SIO_000300: 3.0e-3

MQ
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SIO_000300: 5.89e1

MQRankSum
type: SiteQuality
SIO_000300: 2.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.73e-1

DP
type: SiteQuality
SIO_000300: 2.217893e6

VQSLOD
type: SiteQuality
SIO_000300: -2.694e-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

South Asian
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allele count: 3
allele frequency: 1.822821728034998e-4
allele num: 16458
num of homozygotes: 0

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

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

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

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

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

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

BaseQRankSum
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SIO_000300: -1.175e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 9.9e-2

DP
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SIO_000300: 2.215112e6

FS
type: SiteQuality
SIO_000300: 5.295e0

VQSLOD
type: SiteQuality
SIO_000300: 6.36e-1

QD
type: SiteQuality
SIO_000300: 1.406e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.175e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.2e-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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bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10252
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502313562886846e-5
allele num: 66564
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.215003e6

QD
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SIO_000300: 7.01e0

MQRankSum
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SIO_000300: -6.3e-1

FS
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SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: 1.1e0

VQSLOD
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SIO_000300: 1.94e0

MQ
type: SiteQuality
SIO_000300: 3.732e1

BaseQRankSum
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SIO_000300: -1.044e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.044e0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.036836830757083e-5
allele num: 65858
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15878
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8490
num of homozygotes: 0

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

InbreedingCoeff
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SIO_000300: 1.34e-2

FS
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BaseQRankSum
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SIO_000300: -2.533e0

MQ
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ClippingRankSum
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MQRankSum
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VQSLOD
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DP
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ReadPosRankSum
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15858
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65890
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Latino
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allele num: 11446
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Other
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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ClippingRankSum
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QD
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DP
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FS
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MQ
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VQSLOD
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 65996
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European (Finnish)
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MQ
type: SiteQuality
SIO_000300: 6.006e1

ReadPosRankSum
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InbreedingCoeff
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FS
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DP
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MQRankSum
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QD
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VQSLOD
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BaseQRankSum
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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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African
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num of homozygotes: 0

East Asian
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allele frequency: 7.06547338671691e-4
allele num: 8492
num of homozygotes: 0

European (Non-Finnish)
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6552
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Latino
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

Other
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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QD
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MQ
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VQSLOD
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ReadPosRankSum
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FS
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DP
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 149
bin: 5.75e1
variant carriers: 1

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15996
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.727526618956188e-5
allele num: 11458
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 2.426963565209477e-4
allele num: 65926
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

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

African
type: Population
allele count: 6
allele frequency: 5.82977069568597e-4
allele num: 10292
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.24e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.715e2

BaseQRankSum
type: SiteQuality
SIO_000300: -6.692e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

QD
type: SiteQuality
SIO_000300: 3.0e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

FS
type: SiteQuality
SIO_000300: 2.77816e2

DP
type: SiteQuality
SIO_000300: 2.183723e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.616e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.71e0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512264464809606e-5
allele num: 66126
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16016
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.691e0

FS
type: SiteQuality
SIO_000300: 2.375e0

VQSLOD
type: SiteQuality
SIO_000300: -8.125e-1

QD
type: SiteQuality
SIO_000300: 9.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.13e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.67e0

DP
type: SiteQuality
SIO_000300: 2.172366e6

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.408e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16008
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66142
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.05e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.234e0

VQSLOD
type: SiteQuality
SIO_000300: 1.32e0

QD
type: SiteQuality
SIO_000300: 1.014e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.14e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

DP
type: SiteQuality
SIO_000300: 2.175301e6

FS
type: SiteQuality
SIO_000300: 1.54e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 65
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16002
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.022517757291824e-5
allele num: 66170
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.44e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.09e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.58e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.2e-3

DP
type: SiteQuality
SIO_000300: 2.18557e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.26e-1

QD
type: SiteQuality
SIO_000300: 1.209e1

GenotypeQuality
all individuals: 50
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 4272
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17754
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5086
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.169043722235212e-4
allele num: 8554
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66170
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16002
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.209e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.18557e6

VQSLOD
type: SiteQuality
SIO_000300: 3.58e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-2

GenotypeDepth
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bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 18
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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: 4.25e1
variant carriers: 0

African
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allele count: 5
allele frequency: 4.809542131589073e-4
allele num: 10396
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.737317581653926e-4
allele num: 11512
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16348
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66466
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.34e0

BaseQRankSum
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SIO_000300: -3.417e0

MQRankSum
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SIO_000300: 6.7e-2

MQ
type: SiteQuality
SIO_000300: 5.97e1

InbreedingCoeff
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FS
type: SiteQuality
SIO_000300: 2.131e0

ReadPosRankSum
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QD
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SIO_000300: 1.139e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.9e-2

DP
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SIO_000300: 2.20079e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.009057262359703e-5
allele num: 66466
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.201582e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e0

InbreedingCoeff
type: SiteQuality
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ClippingRankSum
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QD
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FS
type: SiteQuality
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MQRankSum
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VQSLOD
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BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.992e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4293
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504528631179851e-5
allele num: 66466
num of homozygotes: 0

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
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allele num: 66608
num of homozygotes: 0

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

South Asian
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allele frequency: 6.1020258725897e-5
allele num: 16388
num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11534
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Other
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allele frequency: 0.0e0
allele num: 906
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European (Non-Finnish)
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allele count: 3
allele frequency: 4.5092439500977e-5
allele num: 66530
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InbreedingCoeff
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ClippingRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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FS
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BaseQRankSum
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DP
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MQRankSum
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QD
type: SiteQuality
SIO_000300: 1.317e1

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

Latino
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allele frequency: 8.673026886383348e-5
allele num: 11530
num of homozygotes: 0

South Asian
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allele frequency: 5.495847581827064e-4
allele num: 16376
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African
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allele frequency: 0.0e0
allele num: 10398
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8620
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66538
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VQSLOD
type: SiteQuality
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MQRankSum
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FS
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InbreedingCoeff
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MQ
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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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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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66354
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 902
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

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

East Asian
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allele count: 1
allele frequency: 1.162790697674419e-4
allele num: 8600
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South Asian
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allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
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SIO_000300: 1.58e0

MQ
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SIO_000300: 5.957e1

FS
type: SiteQuality
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InbreedingCoeff
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DP
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BaseQRankSum
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QD
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VQSLOD
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MQRankSum
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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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East Asian
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allele count: 1
allele frequency: 1.163873370577281e-4
allele num: 8592
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16218
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 25
allele frequency: 3.765740796529493e-4
allele num: 66388
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6568
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.54e-1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 2.12e0

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

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 6568
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Other
type: Population
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Latino
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allele count: 1
allele frequency: 8.700191404210893e-5
allele num: 11494
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66388
num of homozygotes: 0

South Asian
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allele num: 16218
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BaseQRankSum
type: SiteQuality
SIO_000300: 4.54e-1

FS
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
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SIO_000300: 2.12e0

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.03e-1

ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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Latino
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East Asian
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African
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.012592637223595e-5
allele num: 66388
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 6564
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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Latino
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South Asian
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East Asian
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.015772490123345e-5
allele num: 66318
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ClippingRankSum
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QD
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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DP
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FS
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MQRankSum
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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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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507977199384745e-5
allele num: 66314
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Latino
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European (Finnish)
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East Asian
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allele num: 8586
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African
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Other
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South Asian
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allele count: 1
allele frequency: 6.203473945409429e-5
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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VQSLOD
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DP
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FS
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MQ
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ClippingRankSum
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 4
allele frequency: 2.483546504408295e-4
allele num: 16106
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Other
type: Population
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allele num: 900
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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African
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FS
type: SiteQuality
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InbreedingCoeff
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DP
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QD
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MQRankSum
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MQ
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BaseQRankSum
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ClippingRankSum
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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Other
type: Population
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allele frequency: 2.631578947368421e-2
allele num: 114
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European (Non-Finnish)
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allele count: 193
allele frequency: 5.486071631608869e-2
allele num: 3518
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African
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allele count: 19
allele frequency: 3.612167300380228e-2
allele num: 526
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South Asian
type: Population
allele count: 42
allele frequency: 1.319095477386935e-2
allele num: 3184
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 46
allele frequency: 3.715670436187399e-2
allele num: 1238
num of homozygotes: 0

East Asian
type: Population
allele count: 17
allele frequency: 6.8e-2
allele num: 250
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.252e1

QD
type: SiteQuality
SIO_000300: 1.09e0

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

MQ
type: SiteQuality
SIO_000300: 4.26e1

DP
type: SiteQuality
SIO_000300: 5.09958e5

FS
type: SiteQuality
SIO_000300: 6.2606e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.537e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.613e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.22e-1

Latino
type: Population
allele count: 3
allele frequency: 4.213483146067416e-3
allele num: 712
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.703703703703704e-3
allele num: 540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.10555867490174e-3
allele num: 7124
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 232
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 9.411132024737832e-4
allele num: 7438
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1884
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 3.73e1

DP
type: SiteQuality
SIO_000300: 4.70046e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.98e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.3e0

FS
type: SiteQuality
SIO_000300: 1.6362e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

VQSLOD
type: SiteQuality
SIO_000300: -3.174e0

QD
type: SiteQuality
SIO_000300: 1.0e0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1666
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2090
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2124
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8868
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2660
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.754e0

VQSLOD
type: SiteQuality
SIO_000300: -4.832e0

MQ
type: SiteQuality
SIO_000300: 3.106e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

DP
type: SiteQuality
SIO_000300: 6.2596e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e0

FS
type: SiteQuality
SIO_000300: 8.451000000000001e0

QD
type: SiteQuality
SIO_000300: 7.3e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.38e-2

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 370
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9368
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2712
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.221932114882507e-5
allele num: 19150
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2440
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3004
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.473e0

FS
type: SiteQuality
SIO_000300: 5.021e0

MQRankSum
type: SiteQuality
SIO_000300: -1.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.500000000000001e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.12e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.317e0

MQ
type: SiteQuality
SIO_000300: 3.788e1

QD
type: SiteQuality
SIO_000300: 1.293e1

DP
type: SiteQuality
SIO_000300: 6.94572e5

GenotypeQuality
all individuals: 1877
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.965247301624956e-5
allele num: 33724
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6124
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4870
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4586
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11272
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4136
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 532
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.390000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.678e0

MQ
type: SiteQuality
SIO_000300: 4.024e1

MQRankSum
type: SiteQuality
SIO_000300: -6.37e-1

FS
type: SiteQuality
SIO_000300: 2.447e0

DP
type: SiteQuality
SIO_000300: 8.98349e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.447e0

VQSLOD
type: SiteQuality
SIO_000300: -2.749e0

GenotypeQuality
all individuals: 535
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5300
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6752
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4928
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4394
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 560
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.58663918942126e-5
allele num: 11646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36680
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-2

FS
type: SiteQuality
SIO_000300: 1.537e0

MQRankSum
type: SiteQuality
SIO_000300: 9.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.7e-1

QD
type: SiteQuality
SIO_000300: 5.96e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-3

DP
type: SiteQuality
SIO_000300: 9.36373e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.06e-1

MQ
type: SiteQuality
SIO_000300: 4.018e1

VQSLOD
type: SiteQuality
SIO_000300: -3.114e0

GenotypeQuality
all individuals: 843
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.202546143341703e-5
allele num: 45402
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5180
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5832
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 642
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6472
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12792
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.73e0

VQSLOD
type: SiteQuality
SIO_000300: -2.86e0

MQ
type: SiteQuality
SIO_000300: 3.88e1

MQRankSum
type: SiteQuality
SIO_000300: 8.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.64e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3