8-17932967-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17932967
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17932967
    reference: chr 8
allele count: 1
allele frequency: 8.261595148791329e-6
allele num: 121042
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.173+83A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.125+83A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-71+83A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.173+83A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.139+83A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.131+83A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.173+83A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.125+83A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.156+83A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.711+83A>G
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6168
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13091
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10473
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2672
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10701
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6361
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3697
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum

http://identifiers.org/exac.variant/8-17932968-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17932968
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17932968
    reference: chr 8
allele count: 1
allele frequency: 8.261458643138033e-6
allele num: 121044
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.139+82G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.156+82G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.173+82G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.173+82G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.125+82G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-71+82G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.131+82G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.125+82G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.173+82G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.711+82G>T
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10514
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10721
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13136
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6168
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4087
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2672
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

8-17932968-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17932968
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17932968
    reference: chr 8
allele count: 3
allele frequency: 2.47843759294141e-5
allele num: 121044
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.139+82G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.711+82G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.173+82G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.125+82G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.173+82G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.131+82G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.173+82G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.125+82G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.156+82G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-71+82G>A
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6168
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13136
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10721
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2672
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4087
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10514
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20704
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD

8-17932969-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17932969
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17932969
    reference: chr 8
allele count: 3
allele frequency: 2.477086945751796e-5
allele num: 121110
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.173+81C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.125+81C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-71+81C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.139+81C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.173+81C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.156+81C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.711+81C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.131+81C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.173+81C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.125+81C>T
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13177
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6177
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2729
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2673
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

8-17932970-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17932970
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17932970
    reference: chr 8
allele count: 1
allele frequency: 8.254639107178234e-6
allele num: 121144
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.139+80A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.711+80A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.173+80A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-71+80A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.125+80A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.131+80A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.173+80A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.156+80A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.125+80A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.173+80A>C
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10876
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13201
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10536
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2673
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6382
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3704
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS

8-17932972-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17932972
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17932972
    reference: chr 8
allele count: 18
allele frequency: 1.485369114224885e-4
allele num: 121182
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.173+78G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.156+78G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.131+78G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.711+78G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.173+78G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-71+78G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.139+78G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.125+78G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.173+78G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.125+78G>A
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10555
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6175
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2679
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10923
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13235
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6374
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

8-17932972-CGTTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17932972
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17932968
    reference: chr 8
allele count: 1
allele frequency: 8.252050634582693e-6
allele num: 121182
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.173+74_173+77delAAAC
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-71+74_-71+77delAAAC
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.139+74_139+77delAAAC
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.125+74_125+77delAAAC
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.173+74_173+77delAAAC
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.711+74_711+77delAAAC
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.173+74_173+77delAAAC
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.156+74_156+77delAAAC
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.131+74_131+77delAAAC
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.125+74_125+77delAAAC
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10555
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13235
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6175
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10923
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2679
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4384
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3704
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: CGTTT
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

8-17932975-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17932975
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17932975
    reference: chr 8
allele count: 8
allele frequency: 6.597394029358403e-5
allele num: 121260
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.131+75A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.173+75A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.711+75A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.125+75A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.173+75A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.125+75A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.156+75A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.139+75A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-71+75A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.173+75A>C
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13258
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2673
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10591
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17744
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20723
  bin: 9.75e1
  variant carriers: 8
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-17932983-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17932983
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17932983
    reference: chr 8
allele count: 4
allele frequency: 3.29663084327817e-5
allele num: 121336
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.139+67T>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.131+67T>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.125+67T>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.173+67T>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.156+67T>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.173+67T>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.125+67T>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-71+67T>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.711+67T>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.173+67T>G
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2674
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6184
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10612
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13329
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10988
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2836
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2837
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

8-17932991-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17932991
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17932991
    reference: chr 8
allele count: 2
allele frequency: 1.647772211969417e-5
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.131+59G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.173+59G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.139+59G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.125+59G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.173+59G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.156+59G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.125+59G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-71+59G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.173+59G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.711+59G>A
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10622
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2673
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6432
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum

8-17932993-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17932993
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17932993
    reference: chr 8
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.173+57A>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.139+57A>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.131+57A>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.173+57A>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.156+57A>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.173+57A>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.125+57A>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.125+57A>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.711+57A>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-71+57A>T
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11003
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2673
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum

8-17932997-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17932997
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17932997
    reference: chr 8
allele count: 2
allele frequency: 1.647690761397901e-5
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.125+53C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.173+53C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.173+53C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.139+53C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.173+53C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.131+53C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.156+53C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-71+53C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.125+53C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.711+53C>A
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6184
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2674
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3720
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-17933003-A-ACG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933003
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933005
    reference: chr 8
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: ACG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.139+46_139+47insCG
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.125+46_125+47insCG
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.156+46_156+47insCG
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.173+46_173+47insCG
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.173+46_173+47insCG
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.125+46_125+47insCG
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.131+46_131+47insCG
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.173+46_173+47insCG
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.711+46_711+47insCG
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-71+46_-71+47insCG
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2673
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4087
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13364
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6430
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

8-17933005-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933005
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933005
    reference: chr 8
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.139+45A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.173+45A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.125+45A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.131+45A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.125+45A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.173+45A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.173+45A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.156+45A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.711+45A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-71+45A>G
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13364
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11009
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6187
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2674
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2843
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

8-17933013-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933013
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933013
    reference: chr 8
allele count: 6
allele frequency: 4.942339373970346e-5
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-71+37C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.156+37C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.139+37C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.125+37C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.173+37C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.173+37C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.131+37C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.173+37C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.125+37C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.711+37C>T
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10625
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6187
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4398
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

8-17933025-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933025
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933025
    reference: chr 8
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.131+25A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.125+25A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.173+25A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.711+25A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-71+25A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.173+25A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.173+25A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.156+25A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.139+25A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.125+25A>G
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4087
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13379
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11002
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2675
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6436
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17954
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-17933030-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933030
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933030
    reference: chr 8
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.131+20T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.125+20T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.125+20T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.156+20T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-71+20T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.139+20T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.173+20T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.173+20T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.173+20T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.711+20T>C
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13381
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2674
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17959
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

8-17933034-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933034
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933034
    reference: chr 8
allele count: 3
allele frequency: 2.470966147763776e-5
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.125+16A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.173+16A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.131+16A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.173+16A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-71+16A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.173+16A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.139+16A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.125+16A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.711+16A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.156+16A>G
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6189
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2675
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20723
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD

8-17933036-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933036
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933036
    reference: chr 8
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.125+14A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.125+14A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-71+14A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.156+14A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.173+14A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.139+14A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.173+14A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.173+14A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.711+14A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.131+14A>C
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13383
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2674
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20722
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1787
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17957
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

8-17933039-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933039
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933039
    reference: chr 8
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.711+11A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.156+11A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.125+11A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.139+11A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.173+11A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.131+11A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.173+11A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-71+11A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.125+11A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.173+11A>G
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13383
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2674
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4401
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

8-17933040-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933040
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933040
    reference: chr 8
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.156+10C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.131+10C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.125+10C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.173+10C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.173+10C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.711+10C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.125+10C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.139+10C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-71+10C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.173+10C>T
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13383
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2674
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10998
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17954
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2844
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2836
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

8-17933050-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933050
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933050
    reference: chr 8
allele count: 3
allele frequency: 2.471006852925672e-5
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.139C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.125C>T
  hgvsp: ENSP00000427751.1:p.Thr42Met
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  clinical significance: pathogenic
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.173C>T
  hgvsp: ENSP00000371152.4:p.Thr58Met
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.131C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.173C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.156C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.125C>T
  hgvsp: ENSP00000262097.6:p.Thr42Met
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.173C>T
  hgvsp: ENSP00000326970.10:p.Thr58Ile
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.711C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-71C>T
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13384
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10993
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4087
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Thr58Met
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP

8-17933051-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933051
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933051
    reference: chr 8
allele count: 3
allele frequency: 2.471006852925672e-5
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.124A>G
  hgvsp: ENSP00000427751.1:p.Thr42Ala
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.155A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-72A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.124A>G
  hgvsp: ENSP00000262097.6:p.Thr42Ala
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.172A>G
  hgvsp: ENSP00000371152.4:p.Thr58Ala
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.138A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.172A>G
  hgvsp: ENSP00000326970.10:p.Thr58Ala
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.130A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.172A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.710A>G
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10993
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr58Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

8-17933052-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933052
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933052
    reference: chr 8
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.171A>G
  hgvsp: ENST00000381733.4:c.171A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.171A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.137A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.123A>G
  hgvsp: ENST00000520781.1:c.123A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-73A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.154A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.129A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.123A>G
  hgvsp: ENST00000262097.6:c.123A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.709A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.171A>G
  hgvsp: ENST00000314146.10:c.171A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10993
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.171A>G
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

8-17933058-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933058
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933059
    reference: chr 8
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: TG
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.116dupC
  hgvsp: ENSP00000427751.1:p.Gly40ArgfsTer16
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.130dupC
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.164dupC
  hgvsp: ENSP00000326970.10:p.Gly56ArgfsTer23
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.122dupC
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.116dupC
  hgvsp: ENSP00000262097.6:p.Gly40ArgfsTer16
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-80dupC
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.164dupC
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.164dupC
  hgvsp: ENSP00000371152.4:p.Gly56ArgfsTer16
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.147dupC
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.702dupC
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10994
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13383
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3716
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gly56ArgfsTer16
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD

8-17933062-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933062
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933062
    reference: chr 8
allele count: 2
allele frequency: 1.647365039619129e-5
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.161C>T
  hgvsp: ENSP00000326970.10:p.Pro54Leu
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.113C>T
  hgvsp: ENSP00000427751.1:p.Pro38Leu
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.127C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.699C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.113C>T
  hgvsp: ENSP00000262097.6:p.Pro38Leu
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.161C>T
  hgvsp: ENSP00000371152.4:p.Pro54Leu
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.161C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.119C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.144C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-83C>T
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10992
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6190
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13383
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro54Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/8-17933069-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933069
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933069
    reference: chr 8
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.106T>G
  hgvsp: ENSP00000262097.6:p.Tyr36Asp
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.154T>G
  hgvsp: ENSP00000371152.4:p.Tyr52Asp
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.112T>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.137T>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-90T>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.692T>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.154T>G
  hgvsp: ENSP00000326970.10:p.Tyr52Asp
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.154T>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.120T>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.106T>G
  hgvsp: ENSP00000427751.1:p.Tyr36Asp
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2675
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10987
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4084
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6190
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4400
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17948
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Tyr52Asp
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

8-17933069-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933069
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933069
    reference: chr 8
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.154T>C
  hgvsp: ENSP00000326970.10:p.Tyr52His
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.106T>C
  hgvsp: ENSP00000262097.6:p.Tyr36His
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.106T>C
  hgvsp: ENSP00000427751.1:p.Tyr36His
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.137T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-90T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.692T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.120T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.154T>C
  hgvsp: ENSP00000371152.4:p.Tyr52His
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.112T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.154T>C
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6190
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4084
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2675
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10987
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Tyr52His
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-17933070-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933070
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933070
    reference: chr 8
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.105C>T
  hgvsp: ENST00000262097.6:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.136C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.105C>T
  hgvsp: ENST00000520781.1:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-91C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.691C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.153C>T
  hgvsp: ENST00000314146.10:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.153C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.153C>T
  hgvsp: ENST00000381733.4:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.119C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.111C>T
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6190
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13383
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4084
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17944
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr51Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

8-17933074-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933074
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933074
    reference: chr 8
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.115C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-95C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.149C>A
  hgvsp: ENSP00000326970.10:p.Ser50Ter
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.101C>A
  hgvsp: ENSP00000262097.6:p.Ser34Ter
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.132C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.149C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.149C>A
  hgvsp: ENSP00000371152.4:p.Ser50Ter
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.107C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.101C>A
  hgvsp: ENSP00000427751.1:p.Ser34Ter
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.687C>A
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13383
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2677
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2735
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17946
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3716
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2844
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser50Ter
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

8-17933082-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933082
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933082
    reference: chr 8
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.124C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.679C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.141C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.107C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.93C>A
  hgvsp: ENSP00000427751.1:p.Cys31Ter
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.141C>A
  hgvsp: ENSP00000326970.10:p.Cys47Ter
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.99C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.141C>A
  hgvsp: ENSP00000371152.4:p.Cys47Ter
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.93C>A
  hgvsp: ENSP00000262097.6:p.Cys31Ter
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-103C>A
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4084
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10972
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13381
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2677
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4398
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Cys47Ter
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-17933087-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933087
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933087
    reference: chr 8
allele count: 6
allele frequency: 4.942583653228331e-5
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.88G>T
  hgvsp: ENSP00000262097.6:p.Asp30Tyr
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-108G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.119G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.102G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.88G>T
  hgvsp: ENSP00000427751.1:p.Asp30Tyr
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.94G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.136G>T
  hgvsp: ENSP00000326970.10:p.Asp46Tyr
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.136G>T
  hgvsp: ENSP00000371152.4:p.Asp46Tyr
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.674G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.136G>T
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13367
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4079
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2837
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2835
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp46Tyr
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

8-17933087-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933087
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933087
    reference: chr 8
allele count: 38
allele frequency: 3.130302980377943e-4
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.136G>A
  hgvsp: ENSP00000326970.10:p.Asp46Asn
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.136G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.119G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.674G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.102G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.136G>A
  hgvsp: ENSP00000371152.4:p.Asp46Asn
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.88G>A
  hgvsp: ENSP00000427751.1:p.Asp30Asn
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.94G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.88G>A
  hgvsp: ENSP00000262097.6:p.Asp30Asn
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-108G>A
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4079
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6188
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13367
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 9.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6421
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp46Asn
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

8-17933088-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933088
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933088
    reference: chr 8
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.93G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.135G>A
  hgvsp: ENST00000314146.10:c.135G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.87G>A
  hgvsp: ENST00000262097.6:c.87G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.673G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.118G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.101G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.135G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.87G>A
  hgvsp: ENST00000520781.1:c.87G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.135G>A
  hgvsp: ENST00000381733.4:c.135G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-109G>A
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10961
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13374
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10640
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2680
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3713
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Glu45Glu
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP

8-17933092-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933092
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933092
    reference: chr 8
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.131C>T
  hgvsp: ENSP00000371152.4:p.Thr44Ile
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.89C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.97C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.83C>T
  hgvsp: ENSP00000262097.6:p.Thr28Ile
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.131C>T
  hgvsp: ENSP00000326970.10:p.Thr44Ile
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.114C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.83C>T
  hgvsp: ENSP00000427751.1:p.Thr28Ile
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-113C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.669C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.131C>T
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13371
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2679
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2838
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr44Ile
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

8-17933099-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933099
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933099
    reference: chr 8
allele count: 12908
allele frequency: 1.063805238260067e-1
allele num: 121338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.85-3C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.127-3C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.127-3C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.110-3C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.93-3C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.79-3C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-117-3C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.79-3C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.127-3C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.665-3C>T
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 6.75e1
  variant carriers: 910
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 5.75e1
  variant carriers: 636
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8732
  bin: 3.25e1
  variant carriers: 95
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 6.25e1
  variant carriers: 776
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6614
  bin: 9.75e1
  variant carriers: 4474
genotype depth: GenotypeDepth
  all individuals: 8778
  bin: 2.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 3373
  bin: 4.25e1
  variant carriers: 246
genotype depth: GenotypeDepth
  all individuals: 2424
  bin: 4.75e1
  variant carriers: 362
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 5.25e1
  variant carriers: 507
genotype depth: GenotypeDepth
  all individuals: 11295
  bin: 2.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 8.25e1
  variant carriers: 780
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 7.75e1
  variant carriers: 879
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 9.25e1
  variant carriers: 621
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 8.75e1
  variant carriers: 715
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 7.25e1
  variant carriers: 867
genotype depth: GenotypeDepth
  all individuals: 5012
  bin: 3.75e1
  variant carriers: 147
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: c.127-3C>T
num of homozygotes: 811
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

8-17933102-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933102
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933102
    reference: chr 8
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.127-6T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.79-6T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-117-6T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.127-6T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.79-6T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.110-6T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.665-6T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.127-6T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.93-6T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.85-6T>C
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 11426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13838
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2720
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9132
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
hgvs: c.127-6T>C
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-17933105-CAA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933105
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933103
    reference: chr 8
allele count: 11
allele frequency: 9.065435965056865e-5
allele num: 121340
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-117-11_-117-10delTT
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.93-11_93-10delTT
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.85-11_85-10delTT
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.127-11_127-10delTT
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.127-11_127-10delTT
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.110-11_110-10delTT
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.79-11_79-10delTT
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.127-11_127-10delTT
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.79-11_79-10delTT
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.665-11_665-10delTT
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9127
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2720
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13832
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6493
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11419
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19006
  bin: 9.75e1
  variant carriers: 11
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: CAA
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP

8-17933113-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933113
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933113
    reference: chr 8
allele count: 1
allele frequency: 8.243887157672586e-6
allele num: 121302
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.93-17T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.85-17T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.110-17T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.127-17T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-117-17T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.79-17T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.665-17T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.79-17T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.127-17T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.127-17T>C
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13735
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8954
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2721
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6484
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19136
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

8-17933114-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933114
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933114
    reference: chr 8
allele count: 3
allele frequency: 2.473125370968806e-5
allele num: 121304
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.85-18A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.79-18A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-117-18A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.93-18A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.127-18A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.127-18A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.79-18A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.665-18A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.110-18A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.127-18A>G
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8950
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13731
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6486
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2720
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: T
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

8-17933118-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933118
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933118
    reference: chr 8
allele count: 2
allele frequency: 1.649212501030758e-5
allele num: 121270
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.665-22C>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.127-22C>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.127-22C>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-117-22C>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.85-22C>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.79-22C>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.110-22C>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.93-22C>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.127-22C>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.79-22C>G
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13658
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11364
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6485
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2720
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3500
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2875
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

8-17933136-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933136
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933136
    reference: chr 8
allele count: 384
allele frequency: 3.169676759005514e-3
allele num: 121148
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.79-40A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.93-40A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.110-40A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.665-40A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.127-40A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.127-40A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.127-40A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.79-40A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-117-40A>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.85-40A>G
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4107
  bin: 4.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 4.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 7552
  bin: 2.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 10642
  bin: 3.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 5.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 6.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12326
  bin: 2.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 5.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 6350
  bin: 3.75e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2745
  bin: 9.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1094
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 1
num of homozygotes: 8
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum

8-17933140-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933140
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933140
    reference: chr 8
allele count: 33
allele frequency: 2.725966065852732e-4
allele num: 121058
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.79-44A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.79-44A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.127-44A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.665-44A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.85-44A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.127-44A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.127-44A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.93-44A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.110-44A>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-117-44A>C
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6288
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8357
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 11558
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10158
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4091
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2710
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18960
  bin: 9.75e1
  variant carriers: 33
genotype quality: GenotypeQuality
  all individuals: 5732
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3464
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum

8-17933145-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933145
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933145
    reference: chr 8
allele count: 1
allele frequency: 8.272667107875579e-6
allele num: 120880
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.93-49T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.127-49T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-117-49T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.110-49T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.665-49T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.127-49T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.127-49T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.85-49T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.79-49T>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.79-49T>C
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6217
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1997
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9570
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3397
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9294
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11280
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1377
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1675
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/8-17933146-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933146
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933146
    reference: chr 8
allele count: 2
allele frequency: 1.658787426391308e-5
allele num: 120570
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.93-50G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-117-50G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.85-50G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.127-50G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.110-50G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.79-50G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.79-50G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.127-50G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.127-50G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.665-50G>T
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1982
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11315
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9541
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3395
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4426
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 716
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD

8-17933146-C-CG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933146
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933147
    reference: chr 8
allele count: 1
allele frequency: 8.29393713195654e-6
allele num: 120570
alternate allele: CG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.93-51dupC
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-117-51dupC
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.127-51dupC
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.79-51dupC
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.127-51dupC
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.79-51dupC
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.665-51dupC
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.85-51dupC
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.110-51dupC
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.127-51dupC
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9541
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1982
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11315
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1561
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1080
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 613
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2126
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

8-17933146-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933146
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933146
    reference: chr 8
allele count: 12649
allele frequency: 1.049100107821183e-1
allele num: 120570
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.127-50G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.110-50G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.93-50G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.127-50G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-117-50G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.79-50G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.127-50G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.85-50G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.665-50G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.79-50G>A
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 1.75e1
  variant carriers: 701
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 4.75e1
  variant carriers: 647
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 9.75e1
  variant carriers: 568
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 1.25e1
  variant carriers: 214
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 9.25e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 6.25e1
  variant carriers: 323
genotype depth: GenotypeDepth
  all individuals: 1982
  bin: 5.25e1
  variant carriers: 466
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 3.75e1
  variant carriers: 1420
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 5.75e1
  variant carriers: 367
genotype depth: GenotypeDepth
  all individuals: 9541
  bin: 3.25e1
  variant carriers: 1852
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 8.75e1
  variant carriers: 134
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.5e0
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 9279
  bin: 2.25e1
  variant carriers: 1343
genotype depth: GenotypeDepth
  all individuals: 11315
  bin: 2.75e1
  variant carriers: 1829
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 7.75e1
  variant carriers: 228
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 6.75e1
  variant carriers: 333
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 8.25e1
  variant carriers: 150
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 7.25e1
  variant carriers: 260
genotype depth: GenotypeDepth
  all individuals: 4126
  bin: 4.25e1
  variant carriers: 983
genotype quality: GenotypeQuality
  all individuals: 1131
  bin: 3.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 613
  bin: 2.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 1.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.5e0
  variant carriers: 3
num of homozygotes: 762
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD

8-17933147-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17933147
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17933147
    reference: chr 8
allele count: 21
allele frequency: 1.740571902196436e-4
allele num: 120650
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.85-51C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.79-51C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.665-51C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519545
  gene symbol: ASAH1
  hgvsc: ENST00000519545.1:n.93-51C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-117-51C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.127-51C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.127-51C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.79-51C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.110-51C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.127-51C>T
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6023
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9421
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11601
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4014
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2667
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9440
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2652
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2687
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1998
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3438
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP

8-17941439-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17941439
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17941439
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 57562
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.126+746G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.126+51G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-118+51G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.78+51G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.109+51G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.126+746G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.78+51G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.84+51G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.664+51G>C
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5919
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16458
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20327
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9362
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3235
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2130
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7018
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5087
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

8-17941440-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17941440
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17941440
    reference: chr 8
allele count: 7
allele frequency: 1.219044965344293e-4
allele num: 57422
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.84+50C>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.664+50C>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.126+745C>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.78+50C>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.126+50C>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.78+50C>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.109+50C>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-118+50C>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.126+745C>G
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20322
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9356
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16452
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1893
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6434
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4812
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

8-17941442-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17941442
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17941442
    reference: chr 8
allele count: 9
allele frequency: 1.562554255356089e-4
allele num: 57598
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.78+48C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.664+48C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.109+48C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.84+48C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.126+48C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.126+743C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-118+48C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.126+743C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.78+48C>T
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9281
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5617
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20219
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16551
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4766
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1364
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4198
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13786
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1700
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

8-17941446-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17941446
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17941446
    reference: chr 8
allele count: 1
allele frequency: 1.713854802221156e-5
allele num: 58348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.84+44C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.126+739C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-118+44C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.78+44C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.664+44C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.109+44C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.78+44C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.126+739C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.126+44C>A
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20476
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4856
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2857
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16526
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8715
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4705
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2506
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1756
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5149
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2830
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ

8-17941452-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17941452
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17941452
    reference: chr 8
allele count: 1
allele frequency: 1.659090154959021e-5
allele num: 60274
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.126+733C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.78+38C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.84+38C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.78+38C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.126+733C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.109+38C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.664+38C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-118+38C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.126+38C>A
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5579
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7410
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20951
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15795
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3570
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6320
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1604
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-17941457-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17941457
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17941457
    reference: chr 8
allele count: 3
allele frequency: 4.78484162174232e-5
allele num: 62698
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.109+33G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.78+33G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.84+33G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.126+33G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-118+33G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.664+33G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.126+728G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.126+728G>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.78+33G>T
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6236
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8598
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21265
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 607
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20150
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 874
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8051
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP

8-17941457-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17941457
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17941457
    reference: chr 8
allele count: 1
allele frequency: 1.59494720724744e-5
allele num: 62698
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.126+728G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-118+33G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.109+33G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.78+33G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.126+728G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.664+33G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.78+33G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.84+33G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.126+33G>C
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21265
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6236
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8598
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 950
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6160
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3457
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 999
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5487
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

8-17941459-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17941459
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17941459
    reference: chr 8
allele count: 2
allele frequency: 3.134304967873374e-5
allele num: 63810
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.126+726G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.126+726G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.84+31G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.664+31G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.109+31G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.78+31G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.78+31G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.126+31G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-118+31G>A
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2604
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5823
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10149
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5778
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 612
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1029
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 804
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20042
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

8-17941468-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17941468
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17941468
    reference: chr 8
allele count: 42
allele frequency: 5.830580003887054e-4
allele num: 72034
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.84+22C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.78+22C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-118+22C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.126+717C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.126+717C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.126+22C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.78+22C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.109+22C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.664+22C>T
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19233
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18537
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8016
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 3.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 1204
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3316
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

8-17941474-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17941474
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17941474
    reference: chr 8
allele count: 5
allele frequency: 6.128201985537444e-5
allele num: 81590
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.78+16C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.126+711C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.109+16C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.78+16C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-118+16C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.126+16C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.126+711C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.84+16C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.664+16C>T
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4774
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3786
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14592
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26265
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4212
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 959
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1957
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

8-17941474-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17941474
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17941474
    reference: chr 8
allele count: 1
allele frequency: 1.225640397107489e-5
allele num: 81590
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.126+711C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.78+16C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.664+16C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.84+16C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.126+711C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.126+16C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.78+16C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.109+16C>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-118+16C>A
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14592
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26265
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4774
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3786
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26614
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3616
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1957
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

8-17941481-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17941481
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17941481
    reference: chr 8
allele count: 1
allele frequency: 1.118042977572058e-5
allele num: 89442
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-118+9G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.126+704G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.126+704G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.78+9G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.664+9G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.78+9G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.109+9G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.84+9G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.126+9G>C
  variant of: http://identifiers.org/hgnc/735
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30491
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1154
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4207
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

8-17941483-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17941483
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17941483
    reference: chr 8
allele count: 1
allele frequency: 1.099311830793923e-5
allele num: 90966
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.126+702G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.109+7G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.78+7G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.664+7G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-118+7G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.84+7G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.126+702G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.126+7G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.78+7G>A
  variant of: http://identifiers.org/hgnc/735
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2987
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10424
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31094
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 7.75e1
  variant carriers: 0
hgvs: n.664+7G>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: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

8-17941490-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17941490
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17941490
    reference: chr 8
allele count: 2
allele frequency: 2.120845793302369e-5
allele num: 94302
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.78G>A
  hgvsp: ENST00000520781.1:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.109G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-118G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.126+695G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.664G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.126+695G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.84G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.78G>A
  hgvsp: ENST00000262097.6:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.126G>A
  variant of: http://identifiers.org/hgnc/735
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31771
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2613
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5947
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3163
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 828
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7863
  bin: 2.25e1
  variant carriers: 0
hgvs: n.664G>A
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-17941493-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17941493
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17941493
    reference: chr 8
allele count: 1
allele frequency: 1.038745195803469e-5
allele num: 96270
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-121G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.75G>A
  hgvsp: ENST00000262097.6:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.75G>A
  hgvsp: ENST00000520781.1:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.123G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.126+692G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.81G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.106G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.661G>A
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.126+692G>A
  variant of: http://identifiers.org/hgnc/735
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6477
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7473
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32340
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3290
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2337
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 882
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35164
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Pro25Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum

8-17941496-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17941496
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17941496
    reference: chr 8
allele count: 1
allele frequency: 1.02656756867737e-5
allele num: 97412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.103G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.72G>C
  hgvsp: ENST00000262097.6:c.72G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.126+689G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.72G>C
  hgvsp: ENST00000520781.1:c.72G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.126+689G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-124G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.78G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.120G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.658G>C
  variant of: http://identifiers.org/hgnc/735
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6775
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7045
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32829
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3191
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 777
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 811
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala24Ala
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

8-17941504-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17941504
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17941504
    reference: chr 8
allele count: 7
allele frequency: 6.941827485670084e-5
allele num: 100838
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.64C>T
  hgvsp: ENSP00000262097.6:p.Gln22Ter
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-132C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.126+681C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.70C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.64C>T
  hgvsp: ENSP00000427751.1:p.Gln22Ter
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.95C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.650C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.112C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.126+681C>T
  variant of: http://identifiers.org/hgnc/735
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34242
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5615
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7565
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3208
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gln22Ter
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-17941511-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17941511
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17941511
    reference: chr 8
allele count: 1
allele frequency: 9.740133245022791e-6
allele num: 102668
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.57C>T
  hgvsp: ENST00000520781.1:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.63C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.126+674C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.126+674C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.57C>T
  hgvsp: ENST00000262097.6:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.643C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-139C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.88C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.105C>T
  variant of: http://identifiers.org/hgnc/735
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4902
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3242
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34799
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5082
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala19Ala
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP

8-17941511-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17941511
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17941511
    reference: chr 8
allele count: 1
allele frequency: 9.740133245022791e-6
allele num: 102668
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.63C>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.126+674C>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.57C>G
  hgvsp: ENST00000520781.1:c.57C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-139C>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.88C>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.105C>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.126+674C>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.643C>G
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.57C>G
  hgvsp: ENST00000262097.6:c.57C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/735
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34799
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3242
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4902
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3205
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 490
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5082
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala19Ala
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

8-17941515-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17941515
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17941515
    reference: chr 8
allele count: 1
allele frequency: 9.682041748964022e-6
allele num: 103284
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.84G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.126+670G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-143G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.53G>C
  hgvsp: ENSP00000427751.1:p.Cys18Ser
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.53G>C
  hgvsp: ENSP00000262097.6:p.Cys18Ser
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.126+670G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.59G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.101G>C
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.639G>C
  variant of: http://identifiers.org/hgnc/735
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4716
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8572
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34757
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4661
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4212
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 39577
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Cys18Ser
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

8-17941517-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17941517
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17941517
    reference: chr 8
allele count: 1
allele frequency: 9.67305088024763e-6
allele num: 103380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000519468
  gene symbol: ASAH1
  hgvsc: ENST00000519468.1:n.57C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000523593
  gene symbol: ASAH1
  hgvsc: ENST00000523593.1:n.82C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000427751
  ensembl transcript: ENST00000520781
  gene symbol: ASAH1
  hgvsc: ENST00000520781.1:c.51C>T
  hgvsp: ENST00000520781.1:c.51C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000518087
  gene symbol: ASAH1
  hgvsc: ENST00000518087.2:n.99C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000326970
  ensembl transcript: ENST00000314146
  gene symbol: ASAH1
  hgvsc: ENST00000314146.10:c.126+668C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000371152
  ensembl transcript: ENST00000381733
  gene symbol: ASAH1
  hgvsc: ENST00000381733.4:c.126+668C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000262097
  ensembl transcript: ENST00000262097
  gene symbol: ASAH1
  hgvsc: ENST00000262097.6:c.51C>T
  hgvsp: ENST00000262097.6:c.51C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104763
  ensembl protein: ENSP00000394125
  ensembl transcript: ENST00000417108
  gene symbol: ASAH1
  hgvsc: ENST00000417108.2:c.-145C>T
  variant of: http://identifiers.org/hgnc/735
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104763
  ensembl transcript: ENST00000520051
  gene symbol: ASAH1
  hgvsc: ENST00000520051.1:n.637C>T
  variant of: http://identifiers.org/hgnc/735
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4563
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8788
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34568
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4236
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2913
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser17Ser
num of homozygotes: 0
population: African
reference allele: G

GenotypeQuality
all individuals: 20704
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17248
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2828
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4381
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 169
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1768
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2816
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
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: 11556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66530
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.163061177017911e-4
allele num: 8598
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66532
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11552
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

QD
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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FS
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MQ
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66532
num of homozygotes: 0

East Asian
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allele frequency: 1.162790697674419e-4
allele num: 8600
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South Asian
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num of homozygotes: 0

African
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allele count: 2
allele frequency: 1.928268414963363e-4
allele num: 10372
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 frequency: 0.0e0
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MQRankSum
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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DP
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ClippingRankSum
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MQ
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InbreedingCoeff
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FS
type: SiteQuality
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66566
num of homozygotes: 0

East Asian
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South Asian
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allele frequency: 1.820609297244811e-4
allele num: 16478
num of homozygotes: 0

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

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

Other
type: Population
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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BaseQRankSum
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DP
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MQRankSum
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ClippingRankSum
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MQ
type: SiteQuality
SIO_000300: 5.952e1

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501907422426482e-5
allele num: 66582
num of homozygotes: 0

DP
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
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QD
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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MQ
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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num of homozygotes: 0

African
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Latino
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East Asian
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European (Finnish)
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South Asian
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Other
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MQRankSum
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QD
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FS
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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DP
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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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European (Non-Finnish)
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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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Latino
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Other
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DP
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FS
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MQ
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MQRankSum
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QD
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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South Asian
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East Asian
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African
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Other
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European (Finnish)
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MQRankSum
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FS
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QD
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MQ
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InbreedingCoeff
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DP
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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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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European (Finnish)
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European (Non-Finnish)
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South Asian
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East Asian
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Other
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African
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Latino
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VQSLOD
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MQ
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QD
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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DP
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SIO_000300: 2.484232e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: 1.33e-1

BaseQRankSum
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SIO_000300: -4.22e-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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variant carriers: 2

Other
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num of homozygotes: 0

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

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

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

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

East Asian
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 2.997601918465228e-5
allele num: 66720
num of homozygotes: 0

Latino
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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 frequency: 0.0e0
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FS
type: SiteQuality
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DP
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QD
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MQRankSum
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BaseQRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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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 frequency: 0.0e0
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num of homozygotes: 0

Other
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African
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allele frequency: 0.0e0
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Latino
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European (Non-Finnish)
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allele num: 66732
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QD
type: SiteQuality
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MQ
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BaseQRankSum
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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DP
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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Latino
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num of homozygotes: 0

South Asian
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East Asian
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Other
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European (Non-Finnish)
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African
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European (Finnish)
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FS
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MQRankSum
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MQ
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QD
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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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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East Asian
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European (Non-Finnish)
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Other
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European (Finnish)
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South Asian
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African
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Latino
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MQ
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ReadPosRankSum
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QD
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DP
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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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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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African
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European (Finnish)
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European (Non-Finnish)
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Latino
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Other
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East Asian
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South Asian
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VQSLOD
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InbreedingCoeff
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DP
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QD
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MQRankSum
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ClippingRankSum
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FS
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MQ
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BaseQRankSum
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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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African
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East Asian
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Other
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South Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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InbreedingCoeff
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VQSLOD
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DP
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MQ
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MQRankSum
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BaseQRankSum
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FS
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ReadPosRankSum
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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European (Non-Finnish)
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South Asian
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African
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Other
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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BaseQRankSum
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MQRankSum
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FS
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InbreedingCoeff
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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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South Asian
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African
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Latino
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European (Non-Finnish)
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East Asian
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DP
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ClippingRankSum
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VQSLOD
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QD
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MQ
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FS
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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Latino
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European (Non-Finnish)
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South Asian
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InbreedingCoeff
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MQ
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DP
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BaseQRankSum
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MQRankSum
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FS
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QD
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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ClippingRankSum
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MQ
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InbreedingCoeff
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FS
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DP
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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MQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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European (Finnish)
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European (Non-Finnish)
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African
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Other
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Latino
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FS
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BaseQRankSum
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InbreedingCoeff
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MQ
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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QD
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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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GenotypeQuality
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Latino
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South Asian
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Other
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European (Finnish)
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African
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European (Non-Finnish)
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East Asian
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ReadPosRankSum
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MQRankSum
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MQ
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FS
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InbreedingCoeff
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DP
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BaseQRankSum
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ClippingRankSum
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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European (Non-Finnish)
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African
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Other
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South Asian
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European (Finnish)
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BaseQRankSum
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QD
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FS
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DP
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MQ
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VQSLOD
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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Latino
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European (Finnish)
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African
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South Asian
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FS
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MQ
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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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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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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Other
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East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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VQSLOD
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BaseQRankSum
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MQRankSum
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DP
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ReadPosRankSum
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FS
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InbreedingCoeff
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ClippingRankSum
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QD
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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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African
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Latino
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East Asian
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European (Non-Finnish)
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European (Finnish)
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South Asian
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FS
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ReadPosRankSum
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MQ
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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DP
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ClippingRankSum
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Finnish)
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East Asian
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Other
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European (Non-Finnish)
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allele num: 66736
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DP
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MQ
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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QD
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MQRankSum
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FS
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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Latino
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African
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Other
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East Asian
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European (Finnish)
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DP
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VQSLOD
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MQRankSum
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MQ
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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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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Latino
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East Asian
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European (Non-Finnish)
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South Asian
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Other
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African
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MQ
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VQSLOD
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QD
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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FS
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BaseQRankSum
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ReadPosRankSum
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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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African
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Latino
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East Asian
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Other
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South Asian
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European (Non-Finnish)
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MQ
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DP
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VQSLOD
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BaseQRankSum
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MQRankSum
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QD
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FS
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ClippingRankSum
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InbreedingCoeff
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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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African
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East Asian
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South Asian
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Other
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European (Non-Finnish)
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Latino
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European (Finnish)
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FS
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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MQRankSum
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QD
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DP
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ReadPosRankSum
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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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European (Finnish)
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South Asian
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African
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East Asian
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European (Non-Finnish)
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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SIO_000300: -3.007e0

VQSLOD
type: SiteQuality
SIO_000300: 3.55e0

FS
type: SiteQuality
SIO_000300: 6.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.488973e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

QD
type: SiteQuality
SIO_000300: 1.242e1

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

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

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

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

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

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

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2839
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6429
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20722
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 17930
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4397
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1784
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2837
bin: 9.25e1
variant carriers: 0

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

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
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: 16510
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.17e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

QD
type: SiteQuality
SIO_000300: 1.011e1

FS
type: SiteQuality
SIO_000300: 5.19e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.83e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.48653e6

GenotypeQuality
all individuals: 21
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 17919
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3713
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2837
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6428
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20722
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4391
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1784
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.596e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.593e0

DP
type: SiteQuality
SIO_000300: 2.486368e6

FS
type: SiteQuality
SIO_000300: 4.196e0

MQRankSum
type: SiteQuality
SIO_000300: -4.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.07e1

MQ
type: SiteQuality
SIO_000300: 5.903e1

GenotypeQuality
all individuals: 2823
bin: 8.25e1
variant carriers: 5

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 34
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 15943
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 26975
bin: 9.75e1
variant carriers: 12065

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

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2321
bin: 7.25e1
variant carriers: 6

GenotypeQuality
all individuals: 31
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 69
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3487
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5452
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1360
bin: 8.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2102
bin: 9.25e1
variant carriers: 7

European (Non-Finnish)
type: Population
allele count: 6016
allele frequency: 9.020301676312711e-2
allele num: 66694
num of homozygotes: 308

Other
type: Population
allele count: 97
allele frequency: 1.070640176600442e-1
allele num: 906
num of homozygotes: 6

South Asian
type: Population
allele count: 2213
allele frequency: 1.340887057682986e-1
allele num: 16504
num of homozygotes: 160

African
type: Population
allele count: 1524
allele frequency: 1.465948441708349e-1
allele num: 10396
num of homozygotes: 109

East Asian
type: Population
allele count: 507
allele frequency: 5.858562514444188e-2
allele num: 8654
num of homozygotes: 15

Latino
type: Population
allele count: 1945
allele frequency: 1.680781195990322e-1
allele num: 11572
num of homozygotes: 180

European (Finnish)
type: Population
allele count: 606
allele frequency: 9.165154264972777e-2
allele num: 6612
num of homozygotes: 33

ClippingRankSum
type: SiteQuality
SIO_000300: 7.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.115e0

MQRankSum
type: SiteQuality
SIO_000300: 9.5e-2

QD
type: SiteQuality
SIO_000300: 1.414e1

MQ
type: SiteQuality
SIO_000300: 5.968e1

VQSLOD
type: SiteQuality
SIO_000300: 4.6e0

FS
type: SiteQuality
SIO_000300: 6.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.28e-2

DP
type: SiteQuality
SIO_000300: 3.127728e6

GenotypeQuality
all individuals: 44
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4420
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3503
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19472
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1696
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2889
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2632
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19003
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6846
bin: 6.75e1
variant carriers: 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: 66700
num of homozygotes: 0

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 2.511424e6

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.46e0

FS
type: SiteQuality
SIO_000300: 1.961e1

MQ
type: SiteQuality
SIO_000300: 5.957e1

VQSLOD
type: SiteQuality
SIO_000300: -2.849e0

QD
type: SiteQuality
SIO_000300: 1.831e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.68e-1

GenotypeQuality
all individuals: 35
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19472
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 50
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4416
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2886
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1694
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6837
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2632
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3502
bin: 8.25e1
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: 10392
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 10
allele frequency: 6.059871530723549e-4
allele num: 16502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66700
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.229e0

VQSLOD
type: SiteQuality
SIO_000300: 1.74e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

FS
type: SiteQuality
SIO_000300: 5.421e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.7e-2

MQ
type: SiteQuality
SIO_000300: 5.715e1

QD
type: SiteQuality
SIO_000300: 1.676e1

DP
type: SiteQuality
SIO_000300: 2.511166e6

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4412
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2881
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1694
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3501
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2632
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19002
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6802
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

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

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.461e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 5.06e0

QD
type: SiteQuality
SIO_000300: 1.676e1

MQRankSum
type: SiteQuality
SIO_000300: 1.29e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -3.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e-2

DP
type: SiteQuality
SIO_000300: 2.506859e6

GenotypeQuality
all individuals: 37
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1694
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4414
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6801
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3501
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19152
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2631
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19003
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2882
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.312673450508788e-4
allele num: 8648
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.506941e6

FS
type: SiteQuality
SIO_000300: 2.94e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.59e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.75e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.04e0

QD
type: SiteQuality
SIO_000300: 1.502e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.16e-1

GenotypeQuality
all individuals: 195
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18925
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4408
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 46
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2631
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6761
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1694
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19001
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 2
allele frequency: 1.926040061633282e-4
allele num: 10384
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66662
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.57e-1

DP
type: SiteQuality
SIO_000300: 2.504218e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.715e0

MQRankSum
type: SiteQuality
SIO_000300: 3.03e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.08e0

QD
type: SiteQuality
SIO_000300: 1.338e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.88e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.877e0

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

GenotypeQuality
all individuals: 472
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 374

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2773
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variant carriers: 0

GenotypeQuality
all individuals: 15099
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501726986033939e-5
allele num: 66590
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.207505518763797e-3
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 4.81881264456438e-4
allele num: 10376
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.819063788503517e-4
allele num: 16492
num of homozygotes: 0

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

East Asian
type: Population
allele count: 373
allele frequency: 4.328150382919471e-2
allele num: 8618
num of homozygotes: 8

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.33e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.021e0

DP
type: SiteQuality
SIO_000300: 2.471249e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.25e0

QD
type: SiteQuality
SIO_000300: 1.35e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.2e-2

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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bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502990951994469e-5
allele num: 66534
num of homozygotes: 0

South Asian
type: Population
allele count: 28
allele frequency: 1.698822958378837e-3
allele num: 16482
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.597852441981296e-4
allele num: 11548
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.67e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.53e-1

QD
type: SiteQuality
SIO_000300: 1.473e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

DP
type: SiteQuality
SIO_000300: 2.453883e6

MQRankSum
type: SiteQuality
SIO_000300: 5.2e-2

GenotypeQuality
all individuals: 1929
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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
all individuals: 5485
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GenotypeQuality
all individuals: 2727
bin: 7.25e1
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: 10356
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.51e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.371e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.79e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

DP
type: SiteQuality
SIO_000300: 2.445292e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.79e0

GenotypeQuality
all individuals: 70
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2126
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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
all individuals: 492
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GenotypeQuality
all individuals: 26327
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variant carriers: 2

GenotypeQuality
all individuals: 1561
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variant carriers: 0

GenotypeQuality
all individuals: 1080
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
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: 6606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509844184080203e-5
allele num: 66232
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.0e-1

DP
type: SiteQuality
SIO_000300: 2.444133e6

VQSLOD
type: SiteQuality
SIO_000300: 5.42e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.24e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.524e1

GenotypeQuality
all individuals: 70
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7266
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 60
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3395
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GenotypeQuality
all individuals: 1366
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.075334143377886e-5
allele num: 16460
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

European (Finnish)
type: Population
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: 11474
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66232
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.4e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.52e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.524e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.0e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.42e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.24e-2

DP
type: SiteQuality
SIO_000300: 2.444133e6

GenotypeQuality
all individuals: 2126
bin: 9.25e1
variant carriers: 49

GenotypeQuality
all individuals: 3395
bin: 7.75e1
variant carriers: 50

GenotypeQuality
all individuals: 2451
bin: 4.75e1
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GenotypeQuality
all individuals: 2211
bin: 7.25e1
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GenotypeQuality
all individuals: 492
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variant carriers: 15

GenotypeQuality
all individuals: 135
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GenotypeQuality
all individuals: 60
bin: 7.5e0
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GenotypeQuality
all individuals: 1080
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variant carriers: 18

GenotypeQuality
all individuals: 4426
bin: 6.75e1
variant carriers: 49

GenotypeQuality
all individuals: 2390
bin: 5.25e1
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GenotypeQuality
all individuals: 1561
bin: 3.75e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 11430

GenotypeQuality
all individuals: 716
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variant carriers: 33

GenotypeQuality
all individuals: 7266
bin: 6.25e1
variant carriers: 38

GenotypeQuality
all individuals: 2813
bin: 8.25e1
variant carriers: 58

East Asian
type: Population
allele count: 504
allele frequency: 5.885100420364316e-2
allele num: 8564
num of homozygotes: 15

Other
type: Population
allele count: 94
allele frequency: 1.042128603104213e-1
allele num: 902
num of homozygotes: 5

African
type: Population
allele count: 1345
allele frequency: 1.301780874951607e-1
allele num: 10332
num of homozygotes: 84

European (Finnish)
type: Population
allele count: 605
allele frequency: 9.158340902210112e-2
allele num: 6606
num of homozygotes: 33

South Asian
type: Population
allele count: 2211
allele frequency: 1.343256379100851e-1
allele num: 16460
num of homozygotes: 160

European (Non-Finnish)
type: Population
allele count: 5966
allele frequency: 9.007730402222491e-2
allele num: 66232
num of homozygotes: 294

Latino
type: Population
allele count: 1924
allele frequency: 1.676834582534426e-1
allele num: 11474
num of homozygotes: 171

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.52e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.24e-2

DP
type: SiteQuality
SIO_000300: 2.444133e6

VQSLOD
type: SiteQuality
SIO_000300: 5.42e0

QD
type: SiteQuality
SIO_000300: 1.524e1

GenotypeQuality
all individuals: 52
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18767
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GenotypeQuality
all individuals: 4146
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 684
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GenotypeQuality
all individuals: 3059
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GenotypeQuality
all individuals: 1414
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GenotypeQuality
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GenotypeQuality
all individuals: 1651
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GenotypeQuality
all individuals: 185
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GenotypeQuality
all individuals: 5386
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GenotypeQuality
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GenotypeQuality
all individuals: 568
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7920
bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 2.43161094224924e-4
allele num: 16450
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.46860908775581e-4
allele num: 11532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.659876263769428e-4
allele num: 66270
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.680542110358181e-5
allele num: 10330
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.122e0

FS
type: SiteQuality
SIO_000300: 1.445e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.83e-2

QD
type: SiteQuality
SIO_000300: 1.705e1

DP
type: SiteQuality
SIO_000300: 2.421246e6

GenotypeQuality
all individuals: 6312
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 218
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GenotypeQuality
all individuals: 1748
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 846
bin: 6.25e1
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GenotypeQuality
all individuals: 1862
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GenotypeQuality
all individuals: 4841
bin: 3.75e1
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GenotypeQuality
all individuals: 7271
bin: 1.75e1
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GenotypeQuality
all individuals: 4187
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GenotypeQuality
all individuals: 194
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GenotypeQuality
all individuals: 1240
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GenotypeQuality
all individuals: 125
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GenotypeQuality
all individuals: 11577
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GenotypeQuality
all individuals: 331
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GenotypeQuality
all individuals: 207
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3158
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31590
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3878
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11872
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1736
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.95e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.136e1

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.91e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.776e5

GenotypeQuality
all individuals: 206
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4198
bin: 9.75e1
variant carriers: 8

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 356
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3265
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6474
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6983
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12288
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 8.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11872
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4886
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 1.79763739085773e-3
allele num: 3894
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1694
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 404
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3148
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31524
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.96e-1

QD
type: SiteQuality
SIO_000300: 1.302e1

VQSLOD
type: SiteQuality
SIO_000300: 1.98e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.95e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

DP
type: SiteQuality
SIO_000300: 7.78679e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

GenotypeQuality
all individuals: 6642
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 2057
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5099
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5132
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 8.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 973
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 7.25e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31644
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 2.53968253968254e-3
allele num: 3150
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1722
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.039151712887439e-4
allele num: 4904
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3894
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11886
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.06e-1

DP
type: SiteQuality
SIO_000300: 7.84386e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.218e1

MQRankSum
type: SiteQuality
SIO_000300: 4.95e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.81e0

FS
type: SiteQuality
SIO_000300: 3.086e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.75e-2

GenotypeQuality
all individuals: 112
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1254
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 9.25e1
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GenotypeQuality
all individuals: 16650
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
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variant carriers: 0

GenotypeQuality
all individuals: 2559
bin: 1.25e1
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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
all individuals: 6791
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variant carriers: 0

GenotypeQuality
all individuals: 4198
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3970
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11976
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32034
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 5.733944954128441e-4
allele num: 1744
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3210
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5010
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.74e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.41e-1

DP
type: SiteQuality
SIO_000300: 8.00598e5

VQSLOD
type: SiteQuality
SIO_000300: -1.998e0

QD
type: SiteQuality
SIO_000300: 4.61e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 6788
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5062
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.91131498470948e-4
allele num: 5232
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4170
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33030
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 430
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3370
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12136
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.078e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.68e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 5.85e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.054e0

DP
type: SiteQuality
SIO_000300: 8.36725e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.715e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.49e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.53e-1

GenotypeQuality
all individuals: 990
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3457
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4846
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4204
bin: 9.75e1
variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5487
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 191
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GenotypeQuality
all individuals: 6160
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2082
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4378
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12336
num of homozygotes: 0

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

African
type: Population
allele count: 3
allele frequency: 8.460236886632825e-4
allele num: 3546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34344
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5578
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.667e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.48e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.733e0

VQSLOD
type: SiteQuality
SIO_000300: 7.54e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.344e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.53e-1

DP
type: SiteQuality
SIO_000300: 8.77695e5

GenotypeQuality
all individuals: 8051
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 990
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4204
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 20150
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 874
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 666
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variant carriers: 0

GenotypeQuality
all individuals: 4846
bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.106355382619974e-5
allele num: 12336
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3546
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4378
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34344
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2082
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.667e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.733e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.48e-2

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 8.77695e5

QD
type: SiteQuality
SIO_000300: 1.344e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

GenotypeQuality
all individuals: 581
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 727
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GenotypeQuality
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GenotypeQuality
all individuals: 4693
bin: 2.75e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
all individuals: 4204
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 139
bin: 8.75e1
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GenotypeQuality
all individuals: 527
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5754
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3618
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34938
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2158
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 4.448398576512455e-4
allele num: 4496
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 452
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.11e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.99053e5

BaseQRankSum
type: SiteQuality
SIO_000300: 7.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.445e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.19e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

FS
type: SiteQuality
SIO_000300: 6.419e0

VQSLOD
type: SiteQuality
SIO_000300: 7.66e-1

QD
type: SiteQuality
SIO_000300: 1.291e1

GenotypeQuality
all individuals: 19305
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 7.25e1
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GenotypeQuality
all individuals: 3154
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 476
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GenotypeQuality
all individuals: 439
bin: 1.25e1
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GenotypeQuality
all individuals: 18296
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
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GenotypeQuality
all individuals: 4156
bin: 7.5e0
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GenotypeQuality
all individuals: 209
bin: 5.75e1
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GenotypeQuality
all individuals: 1598
bin: 3.75e1
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GenotypeQuality
all individuals: 214
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4240
bin: 9.75e1
variant carriers: 37

GenotypeQuality
all individuals: 328
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4230
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2666
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 37
allele frequency: 9.388480081197665e-4
allele num: 39410
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 4.324012683770539e-4
allele num: 6938
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5310
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.540357362908195e-4
allele num: 12984
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.83e0

QD
type: SiteQuality
SIO_000300: 1.527e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.17e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-2

FS
type: SiteQuality
SIO_000300: 2.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.26e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.023934e6

VQSLOD
type: SiteQuality
SIO_000300: 3.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

GenotypeQuality
all individuals: 3616
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 455
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GenotypeQuality
all individuals: 369
bin: 4.25e1
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GenotypeQuality
all individuals: 1836
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 1.75e1
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GenotypeQuality
all individuals: 144
bin: 8.75e1
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GenotypeQuality
all individuals: 216
bin: 9.25e1
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GenotypeQuality
all individuals: 14547
bin: 2.25e1
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GenotypeQuality
all individuals: 26614
bin: 6.25e1
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GenotypeQuality
all individuals: 356
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GenotypeQuality
all individuals: 366
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 3.144654088050314e-4
allele num: 3180
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.811594202898551e-3
allele num: 552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.696428571428572e-5
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South Asian
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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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Latino
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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ClippingRankSum
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DP
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QD
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FS
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MQ
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 1.201345506967804e-4
allele num: 8324
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 44800
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Other
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FS
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DP
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MQ
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QD
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 2.032189887823118e-5
allele num: 49208
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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East Asian
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FS
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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MQRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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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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European (Non-Finnish)
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allele num: 50004
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
allele num: 604
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African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
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QD
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MQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: -1.126e0

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

African
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allele frequency: 3.355704697986577e-4
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European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
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Latino
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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QD
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DP
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VQSLOD
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InbreedingCoeff
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MQRankSum
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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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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European (Non-Finnish)
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East Asian
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European (Finnish)
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South Asian
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Latino
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allele num: 10156
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African
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Other
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ClippingRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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ReadPosRankSum
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QD
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MQRankSum
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DP
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FS
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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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African
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South Asian
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East Asian
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European (Finnish)
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European (Non-Finnish)
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allele num: 53382
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Other
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Latino
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ReadPosRankSum
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FS
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MQ
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MQRankSum
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QD
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VQSLOD
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DP
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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South Asian
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East Asian
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African
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Latino
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Other
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MQ
type: SiteQuality
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FS
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QD
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MQRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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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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East Asian
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South Asian
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European (Non-Finnish)
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African
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European (Finnish)
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Latino
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Other
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MQRankSum
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BaseQRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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QD
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MQ
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VQSLOD
type: SiteQuality
SIO_000300: 5.56e-1

DP
type: SiteQuality
SIO_000300: 1.356892e6

GenotypeQuality
all individuals: 218
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 567
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2879
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 523
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39664
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4211
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 159
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7916
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15698
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6810
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.786224635610174e-5
allele num: 55984
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10732
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4828
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 700
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.156e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.56e-1

DP
type: SiteQuality
SIO_000300: 1.356892e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.86e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.21e-1

GenotypeQuality
all individuals: 2950
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3096
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4934
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10774
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7932
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15770
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.77695642902836e-5
allele num: 56276
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6894
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.059e1

VQSLOD
type: SiteQuality
SIO_000300: 5.43e-1

DP
type: SiteQuality
SIO_000300: 1.36474e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.91e-1

GenotypeQuality
all individuals: 4211
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 211
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3024
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 39218
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 561
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6896
num of homozygotes: 0