11-67771535-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67771535
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67771535
    reference: chr 11
allele count: 15
allele frequency: 3.871966959215282e-3
allele num: 3874
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110057
  ensembl protein: ENSP00000437195
  ensembl transcript: ENST00000528423
  gene symbol: UNC93B1
  hgvsc: ENST00000528423.1:c.-117-267C>A
  variant of: http://identifiers.org/hgnc/13481
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110057
  ensembl transcript: ENST00000530138
  gene symbol: UNC93B1
  hgvsc: ENST00000530138.1:n.43C>A
  variant of: http://identifiers.org/hgnc/13481
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110057
  ensembl protein: ENSP00000436758
  ensembl transcript: ENST00000531152
  gene symbol: UNC93B1
  hgvsc: ENST00000531152.1:c.-22C>A
  variant of: http://identifiers.org/hgnc/13481
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110057
  ensembl protein: ENSP00000227471
  ensembl transcript: ENST00000227471
  gene symbol: UNC93B1
  hgvsc: ENST00000227471.2:c.-22C>A
  variant of: http://identifiers.org/hgnc/13481
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110057
  ensembl transcript: ENST00000530331
  gene symbol: UNC93B1
  hgvsc: ENST00000530331.1:n.59C>A
  variant of: http://identifiers.org/hgnc/13481
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 19166
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2648
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14921
  bin: 7.5e0
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4424
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP

11-67771553-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67771553
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67771553
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 2014
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110057
  ensembl protein: ENSP00000227471
  ensembl transcript: ENST00000227471
  gene symbol: UNC93B1
  hgvsc: ENST00000227471.2:c.-40A>G
  variant of: http://identifiers.org/hgnc/13481
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110057
  ensembl protein: ENSP00000437195
  ensembl transcript: ENST00000528423
  gene symbol: UNC93B1
  hgvsc: ENST00000528423.1:c.-117-285A>G
  variant of: http://identifiers.org/hgnc/13481
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110057
  ensembl transcript: ENST00000530331
  gene symbol: UNC93B1
  hgvsc: ENST00000530331.1:n.41A>G
  variant of: http://identifiers.org/hgnc/13481
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110057
  ensembl transcript: ENST00000530138
  gene symbol: UNC93B1
  hgvsc: ENST00000530138.1:n.25A>G
  variant of: http://identifiers.org/hgnc/13481
canonical: true
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18586
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1407
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5782
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 658
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13275
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

11-67771563-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67771563
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67771563
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 1070
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110057
  ensembl protein: ENSP00000227471
  ensembl transcript: ENST00000227471
  gene symbol: UNC93B1
  hgvsc: ENST00000227471.2:c.-50G>A
  variant of: http://identifiers.org/hgnc/13481
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110057
  ensembl transcript: ENST00000530331
  gene symbol: UNC93B1
  hgvsc: ENST00000530331.1:n.31G>A
  variant of: http://identifiers.org/hgnc/13481
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110057
  ensembl transcript: ENST00000530138
  gene symbol: UNC93B1
  hgvsc: ENST00000530138.1:n.15G>A
  variant of: http://identifiers.org/hgnc/13481
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110057
  ensembl protein: ENSP00000437195
  ensembl transcript: ENST00000528423
  gene symbol: UNC93B1
  hgvsc: ENST00000528423.1:c.-117-295G>A
  variant of: http://identifiers.org/hgnc/13481
canonical: true
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19027
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2417
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8387
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11101
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 891
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

11-67782751-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782751
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782751
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 4612
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.109-16C>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.51-16C>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.42-16C>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.-1-16C>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.67-16C>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.-1-16C>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.116-16C>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.27-16C>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.-1-16C>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.-1-16C>G
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13545
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37265
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

11-67782766-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782766
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782766
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 5198
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.67-1G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.-1-1G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.-1-1G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.27-1G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.-1-1G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.109-1G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.116-1G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.-1-1G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.42-1G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.51-1G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.3G>A
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: splice acceptor
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34167
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18056
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
hgvs: c.-1-1G>A
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-67782782-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782782
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782782
    reference: chr 11
allele count: 2
allele frequency: 3.320053120849933e-4
allele num: 6024
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.15G>A
  hgvsp: ENST00000342456.6:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.19G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.15G>A
  hgvsp: ENST00000539229.1:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.42G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.15G>A
  hgvsp: ENST00000316367.6:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.124G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.82G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.15G>A
  hgvsp: ENST00000007633.8:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.57G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.66G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.131G>A
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32005
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20526
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly5Gly
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/11-67782792-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782792
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782792
    reference: chr 11
allele count: 16
allele frequency: 2.410364567640856e-3
allele num: 6638
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.134C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.52C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.67C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.92C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.25C>A
  hgvsp: ENST00000007633.8:c.25C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.29C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.25C>A
  hgvsp: ENST00000342456.6:c.25C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.25C>A
  hgvsp: ENST00000316367.6:c.25C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.141C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.25C>A
  hgvsp: ENST00000539229.1:c.25C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.76C>A
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31035
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21212
  bin: 7.5e0
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 1.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg9Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

11-67782792-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782792
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782792
    reference: chr 11
allele count: 1
allele frequency: 1.506477854775535e-4
allele num: 6638
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.92C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.67C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.25C>T
  hgvsp: ENSP00000474202.1:p.Arg9Trp
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.25C>T
  hgvsp: ENSP00000473990.1:p.Arg9Trp
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.134C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.29C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.25C>T
  hgvsp: ENSP00000474644.1:p.Arg9Trp
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.52C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.25C>T
  hgvsp: ENSP00000474034.1:p.Arg9Trp
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.141C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.76C>T
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21212
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31035
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg9Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: C
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

11-67782793-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782793
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782793
    reference: chr 11
allele count: 1
allele frequency: 1.456452082726478e-4
allele num: 6866
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.26G>A
  hgvsp: ENSP00000474034.1:p.Arg9Gln
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.93G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.26G>A
  hgvsp: ENSP00000473990.1:p.Arg9Gln
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.26G>A
  hgvsp: ENSP00000474644.1:p.Arg9Gln
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.53G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.135G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.68G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.142G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.30G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.26G>A
  hgvsp: ENSP00000474202.1:p.Arg9Gln
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.77G>A
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31006
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21284
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg9Gln
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

11-67782795-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782795
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782795
    reference: chr 11
allele count: 4
allele frequency: 5.72737686139748e-4
allele num: 6984
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.95C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.28C>T
  hgvsp: ENSP00000474034.1:p.Arg10Ter
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.28C>T
  hgvsp: ENSP00000473990.1:p.Arg10Ter
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.144C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.55C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.28C>T
  hgvsp: ENSP00000474644.1:p.Arg10Ter
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.137C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.79C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.70C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.32C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.28C>T
  hgvsp: ENSP00000474202.1:p.Arg10Ter
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21663
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30657
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg10Ter
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

11-67782796-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782796
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782796
    reference: chr 11
allele count: 1
allele frequency: 1.380834023750345e-4
allele num: 7242
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.29G>A
  hgvsp: ENSP00000474644.1:p.Arg10Gln
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.33G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.71G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.80G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.29G>A
  hgvsp: ENSP00000473990.1:p.Arg10Gln
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.29G>A
  hgvsp: ENSP00000474034.1:p.Arg10Gln
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.138G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.145G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.29G>A
  hgvsp: ENSP00000474202.1:p.Arg10Gln
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.96G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.56G>A
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30571
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21767
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg10Gln
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-67782798-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782798
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782798
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 7344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.31C>T
  hgvsp: ENST00000007633.8:c.31C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.82C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.140C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.31C>T
  hgvsp: ENST00000539229.1:c.31C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.35C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.147C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.58C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.98C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.73C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.31C>T
  hgvsp: ENST00000342456.6:c.31C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.31C>T
  hgvsp: ENST00000316367.6:c.31C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21773
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30560
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu11Leu
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-67782809-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782809
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782809
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 8622
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.84C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.42C>A
  hgvsp: ENST00000342456.6:c.42C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.158C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.93C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.109C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.42C>A
  hgvsp: ENST00000539229.1:c.42C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.46C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.42C>A
  hgvsp: ENST00000007633.8:c.42C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.69C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.42C>A
  hgvsp: ENST00000316367.6:c.42C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.151C>A
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20957
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30728
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala14Ala
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum

11-67782815-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782815
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782815
    reference: chr 11
allele count: 1
allele frequency: 1.096491228070175e-4
allele num: 9120
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.48C>T
  hgvsp: ENST00000316367.6:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.75C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.115C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.48C>T
  hgvsp: ENST00000007633.8:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.99C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.52C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.48C>T
  hgvsp: ENST00000342456.6:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.48C>T
  hgvsp: ENST00000539229.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.164C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.157C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.90C>T
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31007
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20257
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His16His
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD

11-67782816-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782816
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782816
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 9466
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.53G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.91G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.100G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.165G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.116G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.49G>A
  hgvsp: ENSP00000474202.1:p.Ala17Thr
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.49G>A
  hgvsp: ENSP00000474034.1:p.Ala17Thr
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.158G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.49G>A
  hgvsp: ENSP00000474644.1:p.Ala17Thr
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.76G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.49G>A
  hgvsp: ENSP00000473990.1:p.Ala17Thr
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30987
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20214
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala17Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
reference allele: G
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

11-67782817-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782817
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782817
    reference: chr 11
allele count: 1
allele frequency: 1.059546514091969e-4
allele num: 9438
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.159C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.50C>T
  hgvsp: ENSP00000473990.1:p.Ala17Val
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.117C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.54C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.50C>T
  hgvsp: ENSP00000474034.1:p.Ala17Val
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.50C>T
  hgvsp: ENSP00000474202.1:p.Ala17Val
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.92C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.50C>T
  hgvsp: ENSP00000474644.1:p.Ala17Val
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.101C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.77C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.166C>T
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31099
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19879
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala17Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum

11-67782823-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782823
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782823
    reference: chr 11
allele count: 1
allele frequency: 9.435742592942064e-5
allele num: 10598
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.165G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.56G>C
  hgvsp: ENSP00000474034.1:p.Arg19Pro
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.60G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.56G>C
  hgvsp: ENSP00000474644.1:p.Arg19Pro
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.56G>C
  hgvsp: ENSP00000474202.1:p.Arg19Pro
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.107G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.172G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.98G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.56G>C
  hgvsp: ENSP00000473990.1:p.Arg19Pro
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.83G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.123G>C
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19357
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31071
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg19Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-67782827-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782827
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782827
    reference: chr 11
allele count: 949
allele frequency: 7.695426532598118e-2
allele num: 12332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.111G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.127G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.102G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.60G>A
  hgvsp: ENST00000007633.8:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.169G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.87G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.60G>A
  hgvsp: ENST00000539229.1:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.176G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.60G>A
  hgvsp: ENST00000316367.6:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.60G>A
  hgvsp: ENST00000342456.6:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.64G>A
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 1.25e1
  variant carriers: 322
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 1.75e1
  variant carriers: 204
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 2.75e1
  variant carriers: 96
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30518
  bin: 2.5e0
  variant carriers: 171
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 3.25e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18934
  bin: 7.5e0
  variant carriers: 723
genotype depth: GenotypeDepth
  all individuals: 2675
  bin: 2.25e1
  variant carriers: 154
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 3.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
hgvs: p.Thr20Thr
num of homozygotes: 57
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

11-67782828-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782828
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782828
    reference: chr 11
allele count: 2
allele frequency: 1.614205004035513e-4
allele num: 12390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.112C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.170C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.61C>T
  hgvsp: ENSP00000474202.1:p.Arg21Trp
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.61C>T
  hgvsp: ENSP00000473990.1:p.Arg21Trp
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.128C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.103C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.61C>T
  hgvsp: ENSP00000474034.1:p.Arg21Trp
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.61C>T
  hgvsp: ENSP00000474644.1:p.Arg21Trp
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.65C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.88C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.177C>T
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18718
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31029
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg21Trp
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

11-67782829-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782829
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782829
    reference: chr 11
allele count: 3
allele frequency: 2.358490566037736e-4
allele num: 12720
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.113G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.62G>A
  hgvsp: ENSP00000474034.1:p.Arg21Gln
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.62G>A
  hgvsp: ENSP00000474644.1:p.Arg21Gln
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.104G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.129G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.171G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.89G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.62G>A
  hgvsp: ENSP00000474202.1:p.Arg21Gln
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.66G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.62G>A
  hgvsp: ENSP00000473990.1:p.Arg21Gln
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.178G>A
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18590
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31094
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg21Gln
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

11-67782840-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782840
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782840
    reference: chr 11
allele count: 1
allele frequency: 6.913716814159292e-5
allele num: 14464
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.189T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.77T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.124T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.73T>C
  hgvsp: ENSP00000474202.1:p.Phe25Leu
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.115T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.140T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.182T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.100T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.73T>C
  hgvsp: ENSP00000473990.1:p.Phe25Leu
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.73T>C
  hgvsp: ENSP00000474644.1:p.Phe25Leu
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.73T>C
  hgvsp: ENSP00000474034.1:p.Phe25Leu
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1602
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31214
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17635
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe25Leu
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP

11-67782843-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782843
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782843
    reference: chr 11
allele count: 4
allele frequency: 2.705993776214315e-4
allele num: 14782
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.76C>T
  hgvsp: ENSP00000474202.1:p.Arg26Trp
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.143C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.76C>T
  hgvsp: ENSP00000474034.1:p.Arg26Trp
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.118C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.185C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.76C>T
  hgvsp: ENSP00000473990.1:p.Arg26Trp
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.76C>T
  hgvsp: ENSP00000474644.1:p.Arg26Trp
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.80C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.192C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.103C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.127C>T
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31208
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17387
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4239
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg26Trp
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD

11-67782845-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782845
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782845
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 15124
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.78G>T
  hgvsp: ENST00000342456.6:c.78G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.194G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.120G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.129G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.78G>T
  hgvsp: ENST00000007633.8:c.78G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.105G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.145G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.78G>T
  hgvsp: ENST00000539229.1:c.78G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.82G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.78G>T
  hgvsp: ENST00000316367.6:c.78G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.187G>T
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4369
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31266
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17279
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg26Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum

11-67782850-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782850
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782850
    reference: chr 11
allele count: 1
allele frequency: 6.40861317610869e-5
allele num: 15604
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.192C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.199C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.83C>T
  hgvsp: ENSP00000474034.1:p.Ala28Val
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.83C>T
  hgvsp: ENSP00000474644.1:p.Ala28Val
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.125C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.83C>T
  hgvsp: ENSP00000473990.1:p.Ala28Val
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.110C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.83C>T
  hgvsp: ENSP00000474202.1:p.Ala28Val
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.134C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.150C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.87C>T
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17089
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4577
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31205
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala28Val
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

11-67782855-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782855
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782855
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 16126
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.197C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.88C>T
  hgvsp: ENSP00000474202.1:p.Leu30Phe
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.88C>T
  hgvsp: ENSP00000473990.1:p.Leu30Phe
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.88C>T
  hgvsp: ENSP00000474034.1:p.Leu30Phe
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.139C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.155C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.130C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.115C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.88C>T
  hgvsp: ENSP00000474644.1:p.Leu30Phe
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.92C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.204C>T
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16824
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu30Phe
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP

11-67782857-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782857
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782857
    reference: chr 11
allele count: 799
allele frequency: 4.84771265623104e-2
allele num: 16482
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.132C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.117C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.157C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.90C>T
  hgvsp: ENST00000539229.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.90C>T
  hgvsp: ENST00000007633.8:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.199C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.90C>T
  hgvsp: ENST00000316367.6:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.94C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.141C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.206C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.90C>T
  hgvsp: ENST00000342456.6:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.25e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 2.75e1
  variant carriers: 142
genotype depth: GenotypeDepth
  all individuals: 16943
  bin: 7.5e0
  variant carriers: 406
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 1.25e1
  variant carriers: 121
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 1.75e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 3.75e1
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 3.25e1
  variant carriers: 109
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30822
  bin: 2.5e0
  variant carriers: 117
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 4624
  bin: 2.25e1
  variant carriers: 120
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu30Leu
num of homozygotes: 28
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/11-67782870-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782870
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782870
    reference: chr 11
allele count: 1
allele frequency: 5.841121495327103e-5
allele num: 17120
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.103C>A
  hgvsp: ENSP00000474644.1:p.Arg35Ser
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.103C>A
  hgvsp: ENSP00000474034.1:p.Arg35Ser
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.170C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.212C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.145C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.154C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.103C>A
  hgvsp: ENSP00000473990.1:p.Arg35Ser
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.130C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.103C>A
  hgvsp: ENSP00000474202.1:p.Arg35Ser
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.219C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.107C>A
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30706
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg35Ser
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

11-67782870-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782870
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782870
    reference: chr 11
allele count: 7
allele frequency: 4.088785046728972e-4
allele num: 17120
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.212C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.145C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.107C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.103C>T
  hgvsp: ENSP00000473990.1:p.Arg35Cys
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.130C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.154C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.103C>T
  hgvsp: ENSP00000474034.1:p.Arg35Cys
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.103C>T
  hgvsp: ENSP00000474644.1:p.Arg35Cys
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.170C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.103C>T
  hgvsp: ENSP00000474202.1:p.Arg35Cys
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.219C>T
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17184
  bin: 7.5e0
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30706
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg35Cys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

11-67782871-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782871
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782871
    reference: chr 11
allele count: 1
allele frequency: 5.801810164771409e-5
allele num: 17236
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.104G>A
  hgvsp: ENSP00000474034.1:p.Arg35His
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.104G>A
  hgvsp: ENSP00000473990.1:p.Arg35His
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.146G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.220G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.108G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.213G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.104G>A
  hgvsp: ENSP00000474644.1:p.Arg35His
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.104G>A
  hgvsp: ENSP00000474202.1:p.Arg35His
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.171G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.155G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.131G>A
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30540
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17433
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4997
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg35His
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS

http://identifiers.org/exac.variant/11-67782879-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782879
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782879
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 17852
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.221C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.116C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.139C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.112C>A
  hgvsp: ENSP00000474644.1:p.Gln38Lys
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.154C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.112C>A
  hgvsp: ENSP00000473990.1:p.Gln38Lys
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.179C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.112C>A
  hgvsp: ENSP00000474034.1:p.Gln38Lys
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.112C>A
  hgvsp: ENSP00000474202.1:p.Gln38Lys
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.163C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.228C>A
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5200
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19087
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29304
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln38Lys
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff

11-67782902-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782902
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782902
    reference: chr 11
allele count: 2
allele frequency: 1.059658789869662e-4
allele num: 18874
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.186C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.202C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.251C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.139C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.135C>T
  hgvsp: ENST00000342456.6:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.135C>T
  hgvsp: ENST00000007633.8:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.135C>T
  hgvsp: ENST00000316367.6:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.135C>T
  hgvsp: ENST00000539229.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.162C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.177C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.244C>T
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24054
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1905
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24543
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His45His
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

11-67782906-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782906
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782906
    reference: chr 11
allele count: 2
allele frequency: 1.044495508669313e-4
allele num: 19148
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.206G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.248G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.139G>A
  hgvsp: ENSP00000474034.1:p.Ala47Thr
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.139G>A
  hgvsp: ENSP00000474644.1:p.Ala47Thr
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.181G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.139G>A
  hgvsp: ENSP00000473990.1:p.Ala47Thr
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.143G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.166G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.139G>A
  hgvsp: ENSP00000474202.1:p.Ala47Thr
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.190G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.255G>A
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24926
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23629
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5026
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala47Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

11-67782906-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782906
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782906
    reference: chr 11
allele count: 1
allele frequency: 5.222477543346563e-5
allele num: 19148
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.255G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.206G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.181G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.143G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.139G>C
  hgvsp: ENSP00000474034.1:p.Ala47Pro
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.139G>C
  hgvsp: ENSP00000473990.1:p.Ala47Pro
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.248G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.166G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.139G>C
  hgvsp: ENSP00000474202.1:p.Ala47Pro
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.190G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.139G>C
  hgvsp: ENSP00000474644.1:p.Ala47Pro
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5026
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23629
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24926
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala47Pro
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

11-67782934-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782934
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782934
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 20974
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+5G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+5G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+5G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+5G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.234G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+5G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+5G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+5G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+5G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+5G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+5G>C
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 20922
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26622
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2838
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.162+5G>C
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-67782935-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782935
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782935
    reference: chr 11
allele count: 1
allele frequency: 4.750142504275128e-5
allele num: 21052
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+6C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+6C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+6C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+6C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+6C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+6C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+6C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.235C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+6C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+6C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+6C>A
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 20865
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26677
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.162+6C>A
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

11-67782939-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782939
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782939
    reference: chr 11
allele count: 1
allele frequency: 4.703668861712135e-5
allele num: 21260
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.239G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+10G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+10G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+10G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+10G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+10G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+10G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+10G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+10G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+10G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+10G>T
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3008
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4648
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1982
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25984
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21247
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

11-67782940-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782940
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782940
    reference: chr 11
allele count: 3
allele frequency: 1.406997467404559e-4
allele num: 21322
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.240G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+11G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+11G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+11G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+11G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+11G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+11G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+11G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+11G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+11G>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+11G>C
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25939
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21252
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

11-67782940-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782940
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782940
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 21322
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+11G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+11G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+11G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+11G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+11G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+11G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.240G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+11G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+11G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+11G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+11G>T
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21252
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25939
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3018
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

11-67782941-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782941
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782941
    reference: chr 11
allele count: 6
allele frequency: 2.82326369282891e-4
allele num: 21252
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.241T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+12T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+12T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+12T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+12T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+12T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+12T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+12T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+12T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+12T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+12T>C
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3086
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21233
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25895
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4635
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

11-67782947-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782947
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782947
    reference: chr 11
allele count: 7456
allele frequency: 2.821890848535312e-1
allele num: 26422
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+18G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+18G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.247G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+18G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+18G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+18G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+18G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+18G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+18G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+18G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+18G>T
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 23772
  bin: 7.5e0
  variant carriers: 6409
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.25e1
  variant carriers: 298
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 2.75e1
  variant carriers: 345
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3427
  bin: 2.25e1
  variant carriers: 378
genotype depth: GenotypeDepth
  all individuals: 5626
  bin: 1.25e1
  variant carriers: 3402
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 3.25e1
  variant carriers: 385
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 18678
  bin: 2.5e0
  variant carriers: 1257
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.75e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 6.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.25e1
  variant carriers: 136
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 1.75e1
  variant carriers: 884
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.75e1
  variant carriers: 111
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 3.75e1
  variant carriers: 375
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.75e1
  variant carriers: 221
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 9.25e1
  variant carriers: 502
num of homozygotes: 746
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

11-67782948-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782948
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782948
    reference: chr 11
allele count: 68
allele frequency: 3.061132619069055e-3
allele num: 22214
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+19T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+19T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+19T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.248T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+19T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+19T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+19T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+19T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+19T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+19T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+19T>C
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3881
  bin: 1.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3768
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24415
  bin: 2.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2490
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 21777
  bin: 7.5e0
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 1.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

11-67782951-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782951
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782951
    reference: chr 11
allele count: 6
allele frequency: 2.724300762804214e-4
allele num: 22024
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+22G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.251G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+22G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+22G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+22G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+22G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+22G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+22G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+22G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+22G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+22G>A
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3735
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3743
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 25053
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21276
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

11-67782969-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782969
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782968
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 19080
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+46delG
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+46delG
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+46delG
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+46delG
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+46delG
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+46delG
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+46delG
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+46delG
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.275delG
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+46delG
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+46delG
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14853
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30960
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2768
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3472
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: AG
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD

11-67782974-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782974
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782974
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 17492
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+45G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+45G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+45G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+45G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+45G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+45G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.274G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+45G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+45G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+45G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+45G>A
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33005
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3480
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12259
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-67782978-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782978
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782978
    reference: chr 11
allele count: 1
allele frequency: 5.781683626271971e-5
allele num: 17296
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+49T>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+49T>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+49T>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+49T>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+49T>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+49T>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+49T>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+49T>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+49T>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.278T>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+49T>G
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11783
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33566
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3517
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

11-67782994-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782994
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782994
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 15118
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+65C>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+65C>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+65C>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+65C>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+65C>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+65C>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+65C>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.294C>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+65C>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+65C>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+65C>G
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35653
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6849
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3496
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD

11-67782999-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67782999
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67782999
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 14776
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+70G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+70G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+70G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+70G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+70G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+70G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+70G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.299G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+70G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+70G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+70G>T
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5747
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35450
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2583
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 716
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

11-67783000-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67783000
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67783000
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 14724
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+71G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+71G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.300G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+71G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+71G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+71G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+71G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+71G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+71G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+71G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+71G>A
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35388
  bin: 2.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3501
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5557
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ

11-67783000-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67783000
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67783000
    reference: chr 11
allele count: 1
allele frequency: 6.791632708503124e-5
allele num: 14724
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.300G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+71G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+71G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+71G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+71G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+71G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+71G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+71G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+71G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+71G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+71G>T
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35388
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5557
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3501
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

11-67783010-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67783010
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67783010
    reference: chr 11
allele count: 3
allele frequency: 2.117148906139732e-4
allele num: 14170
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+81C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.310C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+81C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+81C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+81C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+81C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+81C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+81C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+81C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+81C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+81C>T
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32802
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3436
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3488
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-67783013-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67783013
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67783013
    reference: chr 11
allele count: 4
allele frequency: 2.858367871945119e-4
allele num: 13994
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+84C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+84C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+84C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+84C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+84C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+84C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+84C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.313C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+84C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+84C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+84C>T
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3477
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2560
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32083
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5667
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ

11-67783017-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67783017
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67783017
    reference: chr 11
allele count: 1
allele frequency: 7.216048491845865e-5
allele num: 13858
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+88G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+88G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+88G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+88G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+88G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+88G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+88G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.317G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+88G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+88G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+88G>A
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2568
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30983
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 562
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

11-67783025-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67783025
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67783025
    reference: chr 11
allele count: 100
allele frequency: 7.289692374981776e-3
allele num: 13718
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+96T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.325T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+96T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+96T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+96T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+96T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+96T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+96T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+96T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+96T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+96T>C
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27457
  bin: 2.5e0
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 7.5e0
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 2.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 1
num of homozygotes: 3
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum

11-67783054-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67783054
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67783054
    reference: chr 11
allele count: 1
allele frequency: 7.51653638003608e-5
allele num: 13304
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+125T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+125T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+125T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+125T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+125T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+125T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.354T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+125T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+125T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+125T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+125T>C
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16515
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5593
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum

11-67783055-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67783055
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67783055
    reference: chr 11
allele count: 1
allele frequency: 7.524454477050414e-5
allele num: 13290
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.355A>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+126A>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+126A>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+126A>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+126A>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+126A>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+126A>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+126A>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+126A>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+126A>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+126A>G
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16228
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5593
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-67783056-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67783056
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67783056
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 13280
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+127G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+127G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+127G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+127G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+127G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.356G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+127G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+127G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+127G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+127G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+127G>A
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3342
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15906
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: African
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP

11-67783067-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67783067
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67783067
    reference: chr 11
allele count: 73
allele frequency: 5.553864881314668e-3
allele num: 13144
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.367C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+138C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+138C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+138C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+138C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+138C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+138C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+138C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+138C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+138C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+138C>T
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12741
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 3
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/11-67783103-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67783103
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67783103
    reference: chr 11
allele count: 4
allele frequency: 3.157562361856647e-4
allele num: 12668
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+174C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+174C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+174C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+174C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+174C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+174C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+174C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.403C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+174C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+174C>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+174C>A
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6058
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5489
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

11-67783105-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67783105
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67783105
    reference: chr 11
allele count: 46
allele frequency: 3.630623520126283e-3
allele num: 12670
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+176T>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.405T>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+176T>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+176T>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+176T>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+176T>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+176T>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+176T>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+176T>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+176T>G
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+176T>G
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3167
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5944
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 1
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff

11-67783160-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67783160
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67783160
    reference: chr 11
allele count: 1
allele frequency: 9.317927692881103e-5
allele num: 10732
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+231G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+231G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.460G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+231G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+231G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+231G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+231G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+231G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+231G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+231G>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+231G>T
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2227
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3383
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ

11-67783166-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67783166
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67783166
    reference: chr 11
allele count: 1
allele frequency: 9.782821365681862e-5
allele num: 10222
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+237T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+237T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+237T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+237T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+237T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.466T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+237T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+237T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+237T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+237T>C
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+237T>C
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

11-67783198-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67783198
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67783198
    reference: chr 11
allele count: 2
allele frequency: 2.640612622128334e-4
allele num: 7574
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+269C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+269C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.498C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+269C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+269C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+269C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+269C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+269C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+269C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+269C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+269C>T
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3281
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2820
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

11-67783216-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67783216
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67783216
    reference: chr 11
allele count: 7
allele frequency: 1.262170934006491e-3
allele num: 5546
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.162+287G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.516G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.189+287G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.162+287G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.166+287G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.271+287G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.162+287G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.162+287G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.278+287G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.213+287G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.204+287G>A
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3977
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

11-67785957-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67785957
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67785957
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 20686
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.214-40G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.205-40G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.272-40G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.167-40G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.3257G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.190-285G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.163-40G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.163-40G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.163-285G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.279-40G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.163-40G>A
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9893
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35072
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27547
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

11-67785970-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67785970
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67785970
    reference: chr 11
allele count: 140
allele frequency: 6.59444182760245e-3
allele num: 21230
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.163-27C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.3270C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.214-27C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.163-27C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.190-272C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.167-27C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.279-27C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.163-272C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.205-27C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.163-27C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.272-27C>T
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 33124
  bin: 2.5e0
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 1.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 2.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12795
  bin: 7.5e0
  variant carriers: 108
genotype depth: GenotypeDepth
  all individuals: 2719
  bin: 2.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 3.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3655
  bin: 1.25e1
  variant carriers: 7
num of homozygotes: 3
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum

11-67785986-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67785986
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67785986
    reference: chr 11
allele count: 1
allele frequency: 4.35691878703381e-5
allele num: 22952
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.3286A>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.163-11A>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.167-11A>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.163-11A>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.190-256A>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.272-11A>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.279-11A>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.163-11A>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.214-11A>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.163-256A>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.205-11A>T
  variant of: http://identifiers.org/hgnc/410
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3523
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21438
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25714
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1450
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

11-67786005-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67786005
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67786005
    reference: chr 11
allele count: 1
allele frequency: 3.904724716907458e-5
allele num: 25610
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.280C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.213C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.175C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.222C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.190-237C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.163-237C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.171C>T
  hgvsp: ENST00000316367.6:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.3305C>T
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.171C>T
  hgvsp: ENST00000539229.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.171C>T
  hgvsp: ENST00000007633.8:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.287C>T
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29020
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17680
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3899
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Phe57Phe
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

11-67786006-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67786006
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67786006
    reference: chr 11
allele count: 11
allele frequency: 4.256307073208482e-4
allele num: 25844
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000473990
  ensembl transcript: ENST00000342456
  gene symbol: ALDH3B1
  hgvsc: ENST00000342456.6:c.163-236G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000433100
  gene symbol: ALDH3B1
  hgvsc: ENST00000433100.1:n.288G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000527179
  gene symbol: ALDH3B1
  hgvsc: ENST00000527179.1:n.176G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000529232
  gene symbol: ALDH3B1
  hgvsc: ENST00000529232.1:n.3306G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000525518
  gene symbol: ALDH3B1
  hgvsc: ENST00000525518.1:n.281G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474034
  ensembl transcript: ENST00000539229
  gene symbol: ALDH3B1
  hgvsc: ENST00000539229.1:c.172G>A
  hgvsp: ENSP00000474034.1:p.Glu58Lys
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474202
  ensembl transcript: ENST00000316367
  gene symbol: ALDH3B1
  hgvsc: ENST00000316367.6:c.172G>A
  hgvsp: ENSP00000474202.1:p.Glu58Lys
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000006534
  ensembl protein: ENSP00000474644
  ensembl transcript: ENST00000007633
  gene symbol: ALDH3B1
  hgvsc: ENST00000007633.8:c.172G>A
  hgvsp: ENSP00000474644.1:p.Glu58Lys
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000434449
  gene symbol: ALDH3B1
  hgvsc: ENST00000434449.1:n.214G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000530046
  gene symbol: ALDH3B1
  hgvsc: ENST00000530046.1:n.190-236G>A
  variant of: http://identifiers.org/hgnc/410
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000006534
  ensembl transcript: ENST00000531459
  gene symbol: ALDH3B1
  hgvsc: ENST00000531459.1:n.223G>A
  variant of: http://identifiers.org/hgnc/410
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29270
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 17337
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3903
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2609
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu58Lys
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum

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

GenotypeQuality
all individuals: 310
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 9.75e1
variant carriers: 16

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 72
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African
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Other
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European (Non-Finnish)
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South Asian
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European (Finnish)
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Latino
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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QD
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VQSLOD
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MQ
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FS
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: NaN
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African
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South Asian
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European (Non-Finnish)
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East Asian
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Other
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ClippingRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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FS
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DP
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VQSLOD
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MQRankSum
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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East Asian
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African
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Other
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South Asian
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InbreedingCoeff
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BaseQRankSum
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FS
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DP
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ClippingRankSum
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MQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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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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South Asian
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European (Finnish)
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African
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European (Non-Finnish)
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Other
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East Asian
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Latino
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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QD
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MQ
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InbreedingCoeff
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FS
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DP
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MQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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European (Finnish)
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European (Non-Finnish)
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African
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South Asian
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QD
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MQ
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ClippingRankSum
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DP
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MQRankSum
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VQSLOD
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FS
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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African
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European (Finnish)
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European (Non-Finnish)
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Other
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VQSLOD
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ClippingRankSum
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DP
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BaseQRankSum
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MQ
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MQRankSum
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ReadPosRankSum
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FS
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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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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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African
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European (Finnish)
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Other
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South Asian
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Latino
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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FS
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MQ
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QD
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ReadPosRankSum
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MQRankSum
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DP
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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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South Asian
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European (Finnish)
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Other
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African
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Latino
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QD
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MQ
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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FS
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MQRankSum
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BaseQRankSum
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DP
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ReadPosRankSum
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South Asian
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African
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European (Finnish)
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East Asian
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Latino
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European (Non-Finnish)
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BaseQRankSum
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InbreedingCoeff
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FS
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QD
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DP
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ClippingRankSum
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VQSLOD
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MQ
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SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -4.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.051e0

GenotypeQuality
all individuals: 403
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17997
bin: 2.25e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 2

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 61
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29420
bin: 7.5e0
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.466204506065858e-3
allele num: 1154
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1166
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 440
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3782
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.92399e5

MQRankSum
type: SiteQuality
SIO_000300: 5.44e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.968e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.02e-2

QD
type: SiteQuality
SIO_000300: 1.29e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

FS
type: SiteQuality
SIO_000300: 3.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.44e-1

GenotypeQuality
all individuals: 46
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3856
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 346
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1170
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.564296520423601e-4
allele num: 1322
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.395e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.93e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.720000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.25e-1

DP
type: SiteQuality
SIO_000300: 2.94281e5

VQSLOD
type: SiteQuality
SIO_000300: -2.447e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.84e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.179999999999999e-1

GenotypeQuality
all individuals: 1583
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 50
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1174
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3906
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1372
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.75e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 7.04e0

VQSLOD
type: SiteQuality
SIO_000300: -2.119e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.91e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

DP
type: SiteQuality
SIO_000300: 2.95389e5

ClippingRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

GenotypeQuality
all individuals: 45
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1527
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1244
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4320
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2112
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 474
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 76
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.495e0

VQSLOD
type: SiteQuality
SIO_000300: -2.857e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.99e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e0

QD
type: SiteQuality
SIO_000300: 8.039999999999999e0

DP
type: SiteQuality
SIO_000300: 3.01867e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.495e0

GenotypeQuality
all individuals: 107
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1671
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 350
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 80
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 3.92156862745098e-4
allele num: 2550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4412
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.09e-2

DP
type: SiteQuality
SIO_000300: 3.04101e5

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

FS
type: SiteQuality
SIO_000300: 1.69e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.3e0

QD
type: SiteQuality
SIO_000300: 7.86e0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2768
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 344
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 448
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1234
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.05807e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.38e0

VQSLOD
type: SiteQuality
SIO_000300: -3.198e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.38e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.04e-2

QD
type: SiteQuality
SIO_000300: 7.74e0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

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

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 519
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1242
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.222222222222222e-3
allele num: 450
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4476
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2786
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 356
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.13e-2

MQRankSum
type: SiteQuality
SIO_000300: -7.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

QD
type: SiteQuality
SIO_000300: 6.49e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.05523e5

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 75
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2269
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4778
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 98
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1284
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.794857462269424e-4
allele num: 3578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 458
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

QD
type: SiteQuality
SIO_000300: 3.34e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.481e0

DP
type: SiteQuality
SIO_000300: 3.14493e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.61e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.14e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

GenotypeQuality
all individuals: 2615
bin: 6.25e1
variant carriers: 63

GenotypeQuality
all individuals: 13397
bin: 2.25e1
variant carriers: 71

GenotypeQuality
all individuals: 127
bin: 4.25e1
variant carriers: 14

GenotypeQuality
all individuals: 2768
bin: 1.75e1
variant carriers: 93

GenotypeQuality
all individuals: 28430
bin: 7.5e0
variant carriers: 64

GenotypeQuality
all individuals: 303
bin: 3.75e1
variant carriers: 12

GenotypeQuality
all individuals: 315
bin: 6.75e1
variant carriers: 48

GenotypeQuality
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bin: 7.75e1
variant carriers: 43

GenotypeQuality
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bin: 5.75e1
variant carriers: 65

GenotypeQuality
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bin: 5.25e1
variant carriers: 51

GenotypeQuality
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bin: 2.5e0
variant carriers: 3

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 59

GenotypeQuality
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bin: 8.75e1
variant carriers: 69

GenotypeQuality
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bin: 7.25e1
variant carriers: 46

GenotypeQuality
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bin: 2.75e1
variant carriers: 59

GenotypeQuality
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bin: 4.75e1
variant carriers: 36

GenotypeQuality
all individuals: 119
bin: 8.25e1
variant carriers: 66

GenotypeQuality
all individuals: 74
bin: 9.25e1
variant carriers: 61

GenotypeQuality
all individuals: 870
bin: 9.75e1
variant carriers: 832

East Asian
type: Population
allele count: 16
allele frequency: 3.278688524590164e-2
allele num: 488
num of homozygotes: 0

South Asian
type: Population
allele count: 527
allele frequency: 1.119847003824904e-1
allele num: 4706
num of homozygotes: 19

Other
type: Population
allele count: 4
allele frequency: 3.448275862068965e-2
allele num: 116
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50
num of homozygotes: 0

Latino
type: Population
allele count: 16
allele frequency: 4.166666666666666e-2
allele num: 384
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 54
allele frequency: 1.062155782848151e-2
allele num: 5084
num of homozygotes: 0

African
type: Population
allele count: 332
allele frequency: 2.207446808510638e-1
allele num: 1504
num of homozygotes: 38

FS
type: SiteQuality
SIO_000300: 5.600000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

QD
type: SiteQuality
SIO_000300: 1.426e1

VQSLOD
type: SiteQuality
SIO_000300: 4.21e0

DP
type: SiteQuality
SIO_000300: 3.30568e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.25e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e-1

GenotypeQuality
all individuals: 71
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2033
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29369
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2816
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variant carriers: 2

GenotypeQuality
all individuals: 100
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GenotypeQuality
all individuals: 334
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1416
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5140
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 116
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 4.156275976724855e-4
allele num: 4812
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.06e-1

FS
type: SiteQuality
SIO_000300: 7.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.7e-1

DP
type: SiteQuality
SIO_000300: 3.31617e5

VQSLOD
type: SiteQuality
SIO_000300: 8.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.98e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.33e1

GenotypeQuality
all individuals: 341
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 512
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variant carriers: 1

GenotypeQuality
all individuals: 2628
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variant carriers: 0

GenotypeQuality
all individuals: 2993
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GenotypeQuality
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GenotypeQuality
all individuals: 484
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GenotypeQuality
all individuals: 74
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variant carriers: 4

GenotypeQuality
all individuals: 29432
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 14015
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GenotypeQuality
all individuals: 2443
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variant carriers: 0

GenotypeQuality
all individuals: 110
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GenotypeQuality
all individuals: 1961
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 86
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GenotypeQuality
all individuals: 25
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GenotypeQuality
all individuals: 374
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variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 4.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4998
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.716463414634146e-4
allele num: 5248
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 392
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1416
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 492
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.33874e5

QD
type: SiteQuality
SIO_000300: 8.99e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.01e-1

FS
type: SiteQuality
SIO_000300: 4.883e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.98e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 5.89e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.395e0

MQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

GenotypeQuality
all individuals: 13000
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
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variant carriers: 0

GenotypeQuality
all individuals: 94
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GenotypeQuality
all individuals: 101
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GenotypeQuality
all individuals: 234
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GenotypeQuality
all individuals: 2475
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variant carriers: 0

GenotypeQuality
all individuals: 2632
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variant carriers: 0

GenotypeQuality
all individuals: 29431
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GenotypeQuality
all individuals: 73
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GenotypeQuality
all individuals: 4158
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GenotypeQuality
all individuals: 93
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variant carriers: 1

GenotypeQuality
all individuals: 441
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GenotypeQuality
all individuals: 387
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variant carriers: 0

GenotypeQuality
all individuals: 2042
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GenotypeQuality
all individuals: 115
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GenotypeQuality
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GenotypeQuality
all individuals: 23
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GenotypeQuality
all individuals: 151
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GenotypeQuality
all individuals: 83
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GenotypeQuality
all individuals: 28
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1446
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 146
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 520
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5824
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.392344497607655e-3
allele num: 418
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.12e-1

QD
type: SiteQuality
SIO_000300: 1.252e1

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.97e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

DP
type: SiteQuality
SIO_000300: 3.50146e5

GenotypeQuality
all individuals: 92
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variant carriers: 0

GenotypeQuality
all individuals: 414
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 397
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GenotypeQuality
all individuals: 227
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1446
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 152
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.759040216289286e-4
allele num: 5918
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 522
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6274
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.03e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.441e0

VQSLOD
type: SiteQuality
SIO_000300: 1.43e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.73e-1

DP
type: SiteQuality
SIO_000300: 3.54411e5

MQRankSum
type: SiteQuality
SIO_000300: 5.3e-2

QD
type: SiteQuality
SIO_000300: 1.332e1

GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 206
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 406
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GenotypeQuality
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GenotypeQuality
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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: 33
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6434
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1450
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 424
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6042
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.638e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.97e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.41e-1

DP
type: SiteQuality
SIO_000300: 3.5634e5

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

GenotypeQuality
all individuals: 4787
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
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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
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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: 28
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GenotypeQuality
all individuals: 12320
bin: 2.25e1
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GenotypeQuality
all individuals: 368
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GenotypeQuality
all individuals: 78
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GenotypeQuality
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GenotypeQuality
all individuals: 94
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GenotypeQuality
all individuals: 117
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GenotypeQuality
all individuals: 188
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variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.48720999405116e-4
allele num: 6724
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 160
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 422
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6190
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1476
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.007e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

FS
type: SiteQuality
SIO_000300: 1.871e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.058e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.62528e5

GenotypeQuality
all individuals: 2942
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28995
bin: 7.5e0
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 2.75e1
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GenotypeQuality
all individuals: 66
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2921
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2403
bin: 2.5e0
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GenotypeQuality
all individuals: 11431
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 608
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 9.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 432
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 158
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1496
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 90
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6380
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6992
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.093e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.136e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.96e-2

QD
type: SiteQuality
SIO_000300: 9.18e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.3e0

DP
type: SiteQuality
SIO_000300: 3.66322e5

GenotypeQuality
all individuals: 164
bin: 7.75e1
variant carriers: 20

GenotypeQuality
all individuals: 28442
bin: 7.5e0
variant carriers: 47

GenotypeQuality
all individuals: 116
bin: 5.25e1
variant carriers: 15

GenotypeQuality
all individuals: 2797
bin: 1.25e1
variant carriers: 26

GenotypeQuality
all individuals: 2826
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 110
bin: 8.25e1
variant carriers: 22

GenotypeQuality
all individuals: 348
bin: 2.75e1
variant carriers: 35

GenotypeQuality
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variant carriers: 41

GenotypeQuality
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bin: 8.75e1
variant carriers: 43

GenotypeQuality
all individuals: 812
bin: 9.75e1
variant carriers: 769

GenotypeQuality
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variant carriers: 37

GenotypeQuality
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bin: 3.75e1
variant carriers: 5

GenotypeQuality
all individuals: 72
bin: 9.25e1
variant carriers: 46

GenotypeQuality
all individuals: 320
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variant carriers: 29

GenotypeQuality
all individuals: 90
bin: 4.75e1
variant carriers: 10

GenotypeQuality
all individuals: 591
bin: 6.75e1
variant carriers: 39

GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 11392
bin: 2.25e1
variant carriers: 43

GenotypeQuality
all individuals: 4834
bin: 6.25e1
variant carriers: 41

GenotypeQuality
all individuals: 201
bin: 7.25e1
variant carriers: 25

East Asian
type: Population
allele count: 14
allele frequency: 2.348993288590604e-2
allele num: 596
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 90
num of homozygotes: 0

South Asian
type: Population
allele count: 576
allele frequency: 8.058198097369894e-2
allele num: 7148
num of homozygotes: 21

African
type: Population
allele count: 153
allele frequency: 9.646910466582598e-2
allele num: 1586
num of homozygotes: 7

European (Non-Finnish)
type: Population
allele count: 46
allele frequency: 7.12294828120161e-3
allele num: 6458
num of homozygotes: 0

Latino
type: Population
allele count: 7
allele frequency: 1.576576576576576e-2
allele num: 444
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 1.875e-2
allele num: 160
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.68e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.107e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.14e-2

QD
type: SiteQuality
SIO_000300: 1.287e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

DP
type: SiteQuality
SIO_000300: 3.74436e5

GenotypeQuality
all individuals: 206
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5574
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3028
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
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variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
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variant carriers: 0

GenotypeQuality
all individuals: 95
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variant carriers: 0

GenotypeQuality
all individuals: 11292
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 7.75e1
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GenotypeQuality
all individuals: 684
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2585
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3306
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28394
bin: 7.5e0
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 166
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 444
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.471453796350795e-4
allele num: 6796
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1596
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 102
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

DP
type: SiteQuality
SIO_000300: 3.83112e5

FS
type: SiteQuality
SIO_000300: 2.48e0

QD
type: SiteQuality
SIO_000300: 1.312e1

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 56
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 33
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 89
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 335
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3306
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 684
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variant carriers: 0

GenotypeQuality
all individuals: 11292
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 106
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variant carriers: 1

GenotypeQuality
all individuals: 128
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 206
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variant carriers: 5

GenotypeQuality
all individuals: 255
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variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 5.25e1
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GenotypeQuality
all individuals: 3028
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5574
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2585
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 95
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 184
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 28394
bin: 7.5e0
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 444
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.414361389052384e-4
allele num: 6796
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7398
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 102
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 2.506265664160401e-3
allele num: 1596
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 166
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.48e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.07e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 1.312e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

DP
type: SiteQuality
SIO_000300: 3.83112e5

GenotypeQuality
all individuals: 2495
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2951
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 681
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variant carriers: 0

GenotypeQuality
all individuals: 2916
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
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variant carriers: 0

GenotypeQuality
all individuals: 343
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variant carriers: 0

GenotypeQuality
all individuals: 49
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variant carriers: 0

GenotypeQuality
all individuals: 205
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variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28437
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variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11957
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5668
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variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 5.25e1
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GenotypeQuality
all individuals: 106
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 77
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 32
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.597444089456869e-3
allele num: 626
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7450
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1606
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 108
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6832
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.72e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.171e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.91e-2

DP
type: SiteQuality
SIO_000300: 3.87173e5

QD
type: SiteQuality
SIO_000300: 5.84e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.067e0

FS
type: SiteQuality
SIO_000300: 3.645e0

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 38
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 193
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GenotypeQuality
all individuals: 33
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GenotypeQuality
all individuals: 34
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variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 170
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7154
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1638
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 116
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 668
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 494
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.03581e5

QD
type: SiteQuality
SIO_000300: 1.11e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 7.782e0

VQSLOD
type: SiteQuality
SIO_000300: -1.111e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.52e-2

GenotypeQuality
all individuals: 80
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23501
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 1880
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
all individuals: 325
bin: 3.25e1
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GenotypeQuality
all individuals: 757
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20148
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 168
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1698
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.290322580645161e-4
allele num: 7750
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 146
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.287995878413189e-4
allele num: 7764
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.329e1

DP
type: SiteQuality
SIO_000300: 4.37292e5

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 1.772e1

VQSLOD
type: SiteQuality
SIO_000300: -1.169e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.65e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

GenotypeQuality
all individuals: 166
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5840
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.25e1
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GenotypeQuality
all individuals: 55
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GenotypeQuality
all individuals: 1254
bin: 2.5e0
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GenotypeQuality
all individuals: 34
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GenotypeQuality
all individuals: 1688
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21561
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22794
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2502
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
all individuals: 46
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 154
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 576
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 5.91016548463357e-4
allele num: 1692
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 174
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.255965837729214e-4
allele num: 7962
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7776
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.811e-1

QD
type: SiteQuality
SIO_000300: 1.022e1

FS
type: SiteQuality
SIO_000300: 3.729e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.63e-2

DP
type: SiteQuality
SIO_000300: 4.43852e5

GenotypeQuality
all individuals: 2502
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5840
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 3.75e1
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GenotypeQuality
all individuals: 36
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 9.25e1
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 110
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21561
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 174
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1692
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 576
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.286008230452675e-4
allele num: 7776
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 154
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7962
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.811e-1

FS
type: SiteQuality
SIO_000300: 3.729e0

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.63e-2

QD
type: SiteQuality
SIO_000300: 1.022e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.43852e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

GenotypeDepth
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1875
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 711
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1106
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 252
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1622
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7952
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9132
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

FS
type: SiteQuality
SIO_000300: 7.701e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.517e0

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 4.79e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.897e0

DP
type: SiteQuality
SIO_000300: 4.60574e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.87e-1

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

GenotypeQuality
all individuals: 44
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variant carriers: 0

GenotypeQuality
all individuals: 1846
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2432
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 4.25e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 80
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7960
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9198
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.385041551246537e-3
allele num: 722
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1628
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1102
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 250
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.62e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.01e0

VQSLOD
type: SiteQuality
SIO_000300: -3.126e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.06e-2

DP
type: SiteQuality
SIO_000300: 4.61669e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.666e0

QD
type: SiteQuality
SIO_000300: 1.99e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.57e0

GenotypeQuality
all individuals: 188
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
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variant carriers: 1

GenotypeQuality
all individuals: 21199
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GenotypeQuality
all individuals: 922
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GenotypeQuality
all individuals: 120
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 34
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GenotypeQuality
all individuals: 285
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variant carriers: 0

GenotypeQuality
all individuals: 771
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variant carriers: 0

GenotypeQuality
all individuals: 5476
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 146
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 8.25e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1640
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7964
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 272
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1128
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.070893124866138e-4
allele num: 9338
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 726
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 4.58329e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.21e-1

QD
type: SiteQuality
SIO_000300: 6.21e0

GenotypeQuality
all individuals: 5468
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 292
bin: 3.75e1
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GenotypeQuality
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variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 3.95778364116095e-3
allele num: 758
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9352
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7970
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 274
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1136
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

FS
type: SiteQuality
SIO_000300: 7.847e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.87e-1

QD
type: SiteQuality
SIO_000300: 1.362e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.49e-2

DP
type: SiteQuality
SIO_000300: 4.58417e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.78e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.327e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 81
bin: 9.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9352
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7970
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 758
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1640
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 274
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1136
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.362e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.49e-2

FS
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
type: SiteQuality
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MQRankSum
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VQSLOD
type: SiteQuality
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DP
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SIO_000300: 4.58417e5

GenotypeQuality
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variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7960
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1132
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 270
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 3.645200486026731e-3
allele num: 1646
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 732
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.153e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.03e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.54e-1

DP
type: SiteQuality
SIO_000300: 4.5829e5

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

GenotypeQuality
all individuals: 582
bin: 5.75e1
variant carriers: 509

GenotypeQuality
all individuals: 303
bin: 4.75e1
variant carriers: 192

GenotypeQuality
all individuals: 330
bin: 7.75e1
variant carriers: 280

GenotypeQuality
all individuals: 1294
bin: 1.25e1
variant carriers: 511

GenotypeQuality
all individuals: 369
bin: 8.25e1
variant carriers: 354

GenotypeQuality
all individuals: 476
bin: 7.25e1
variant carriers: 406

GenotypeQuality
all individuals: 481
bin: 5.25e1
variant carriers: 330

GenotypeQuality
all individuals: 2525
bin: 1.75e1
variant carriers: 897

GenotypeQuality
all individuals: 5913
bin: 9.75e1
variant carriers: 5909

GenotypeQuality
all individuals: 4386
bin: 6.25e1
variant carriers: 661

GenotypeQuality
all individuals: 5994
bin: 2.5e0
variant carriers: 29

GenotypeQuality
all individuals: 192
bin: 4.25e1
variant carriers: 129

GenotypeQuality
all individuals: 276
bin: 3.75e1
variant carriers: 149

GenotypeQuality
all individuals: 13617
bin: 2.25e1
variant carriers: 822

GenotypeQuality
all individuals: 940
bin: 2.75e1
variant carriers: 589

GenotypeQuality
all individuals: 484
bin: 8.75e1
variant carriers: 479

GenotypeQuality
all individuals: 1013
bin: 6.75e1
variant carriers: 673

GenotypeQuality
all individuals: 15978
bin: 7.5e0
variant carriers: 495

GenotypeQuality
all individuals: 814
bin: 3.25e1
variant carriers: 547

European (Finnish)
type: Population
allele count: 256
allele frequency: 4.60431654676259e-1
allele num: 556
num of homozygotes: 32

Latino
type: Population
allele count: 361
allele frequency: 3.305860805860806e-1
allele num: 1092
num of homozygotes: 28

South Asian
type: Population
allele count: 1602
allele frequency: 1.946064139941691e-1
allele num: 8232
num of homozygotes: 163

African
type: Population
allele count: 327
allele frequency: 1.822742474916388e-1
allele num: 1794
num of homozygotes: 25

European (Non-Finnish)
type: Population
allele count: 4307
allele frequency: 3.32895347039728e-1
allele num: 12938
num of homozygotes: 429

East Asian
type: Population
allele count: 536
allele frequency: 3.379571248423707e-1
allele num: 1586
num of homozygotes: 58

Other
type: Population
allele count: 67
allele frequency: 2.991071428571428e-1
allele num: 224
num of homozygotes: 11

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.54e1

MQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.06e-2

FS
type: SiteQuality
SIO_000300: 5.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 5.21371e5

VQSLOD
type: SiteQuality
SIO_000300: 3.98e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

GenotypeQuality
all individuals: 127
bin: 9.75e1
variant carriers: 107

GenotypeQuality
all individuals: 2876
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 19499
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variant carriers: 1

GenotypeQuality
all individuals: 24
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variant carriers: 1

GenotypeQuality
all individuals: 174
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variant carriers: 3

GenotypeQuality
all individuals: 114
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variant carriers: 2

GenotypeQuality
all individuals: 225
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variant carriers: 0

GenotypeQuality
all individuals: 96
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GenotypeQuality
all individuals: 5338
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variant carriers: 0

GenotypeQuality
all individuals: 24078
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variant carriers: 2

GenotypeQuality
all individuals: 1277
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variant carriers: 4

GenotypeQuality
all individuals: 1275
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 4

GenotypeQuality
all individuals: 700
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 673
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 169
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 136
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variant carriers: 1

GenotypeQuality
all individuals: 200
bin: 5.25e1
variant carriers: 3

GenotypeQuality
all individuals: 54
bin: 8.25e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.002405773857257e-4
allele num: 9976
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 300
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.243781094527363e-3
allele num: 804
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8008
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1282
num of homozygotes: 0

African
type: Population
allele count: 66
allele frequency: 4.014598540145985e-2
allele num: 1644
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.769e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.35e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e-1

DP
type: SiteQuality
SIO_000300: 4.4491e5

FS
type: SiteQuality
SIO_000300: 1.107e0

VQSLOD
type: SiteQuality
SIO_000300: 4.82e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.57e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1214
bin: 1.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 19940
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variant carriers: 0

GenotypeQuality
all individuals: 924
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variant carriers: 0

GenotypeQuality
all individuals: 59
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variant carriers: 0

GenotypeQuality
all individuals: 50
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variant carriers: 0

GenotypeQuality
all individuals: 2124
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variant carriers: 1

GenotypeQuality
all individuals: 690
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variant carriers: 2

GenotypeQuality
all individuals: 474
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variant carriers: 0

GenotypeQuality
all individuals: 174
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GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 137
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variant carriers: 1

GenotypeQuality
all individuals: 701
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GenotypeQuality
all individuals: 24922
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GenotypeQuality
all individuals: 211
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GenotypeQuality
all individuals: 138
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variant carriers: 0

GenotypeQuality
all individuals: 5465
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variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 124
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 302
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8008
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 3.778337531486146e-3
allele num: 1588
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 196
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1272
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9862
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.40452e5

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.939e1

FS
type: SiteQuality
SIO_000300: 6.103e0

VQSLOD
type: SiteQuality
SIO_000300: -7.559e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.67e-2

GenotypeQuality
all individuals: 1581
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5352
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12815
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variant carriers: 1

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 47
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variant carriers: 0

GenotypeQuality
all individuals: 30560
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variant carriers: 0

GenotypeQuality
all individuals: 159
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variant carriers: 0

GenotypeQuality
all individuals: 1266
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variant carriers: 0

GenotypeQuality
all individuals: 1903
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variant carriers: 0

GenotypeQuality
all individuals: 156
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variant carriers: 1

GenotypeQuality
all individuals: 298
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variant carriers: 0

GenotypeQuality
all individuals: 416
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variant carriers: 0

GenotypeQuality
all individuals: 619
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variant carriers: 0

GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 111
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variant carriers: 0

GenotypeQuality
all individuals: 33
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variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 97
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variant carriers: 0

GenotypeQuality
all individuals: 117
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7844
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7988
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1322
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 982
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 208
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.67e0

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.419999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.73e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.88544e5

QD
type: SiteQuality
SIO_000300: 3.46e0

GenotypeQuality
all individuals: 12
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 1

GenotypeQuality
all individuals: 2068
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variant carriers: 0

GenotypeQuality
all individuals: 5286
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variant carriers: 0

GenotypeQuality
all individuals: 131
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GenotypeQuality
all individuals: 252
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GenotypeQuality
all individuals: 1359
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variant carriers: 0

GenotypeQuality
all individuals: 32145
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GenotypeQuality
all individuals: 602
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GenotypeQuality
all individuals: 73
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variant carriers: 1

GenotypeQuality
all individuals: 2131
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variant carriers: 0

GenotypeQuality
all individuals: 344
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variant carriers: 1

GenotypeQuality
all individuals: 102
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variant carriers: 0

GenotypeQuality
all individuals: 9213
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 161
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variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 140
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6934
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 174
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.61291e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.97e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.451e-1

QD
type: SiteQuality
SIO_000300: 8.289999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

FS
type: SiteQuality
SIO_000300: 2.291e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 1903
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GenotypeQuality
all individuals: 104
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 30
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 291
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variant carriers: 0

GenotypeQuality
all individuals: 1175
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variant carriers: 0

GenotypeQuality
all individuals: 57
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variant carriers: 0

GenotypeQuality
all individuals: 67
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variant carriers: 0

GenotypeQuality
all individuals: 97
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variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 33
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variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 1

GenotypeQuality
all individuals: 597
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7798
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1192
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.256281407035176e-3
allele num: 796
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 128
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6800
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 172
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.04e-2

QD
type: SiteQuality
SIO_000300: 9.789999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.82e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.2e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.854e0

DP
type: SiteQuality
SIO_000300: 3.57335e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 34423
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GenotypeQuality
all individuals: 29
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GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 824
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GenotypeQuality
all individuals: 18
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GenotypeQuality
all individuals: 2334
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GenotypeQuality
all individuals: 879
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GenotypeQuality
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GenotypeQuality
all individuals: 119
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GenotypeQuality
all individuals: 53
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GenotypeQuality
all individuals: 5657
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 15
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 76
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7692
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 504
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 304
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 978
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5408
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.191e1

DP
type: SiteQuality
SIO_000300: 3.108e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.169999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.56e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.268e0

GenotypeQuality
all individuals: 114
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
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variant carriers: 0

GenotypeQuality
all individuals: 15
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GenotypeQuality
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GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 28
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variant carriers: 0

GenotypeQuality
all individuals: 99
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GenotypeQuality
all individuals: 92
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GenotypeQuality
all individuals: 565
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GenotypeQuality
all individuals: 19
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GenotypeQuality
all individuals: 637
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GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 14
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GenotypeQuality
all individuals: 34299
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variant carriers: 1

GenotypeQuality
all individuals: 19
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GenotypeQuality
all individuals: 159
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 154
num of homozygotes: 0

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

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 934
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5202
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.99787e5

VQSLOD
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SIO_000300: 2.77e0

QD
type: SiteQuality
SIO_000300: 1.382e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.34e-2

GenotypeQuality
all individuals: 100
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 3

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 1

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

European (Non-Finnish)
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allele count: 0
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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 274
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

Other
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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FS
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BaseQRankSum
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DP
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InbreedingCoeff
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SIO_000300: 6.14e-2

MQRankSum
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ClippingRankSum
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QD
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VQSLOD
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MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele count: 1
allele frequency: 1.077586206896552e-3
allele num: 928
num of homozygotes: 0

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

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

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

South Asian
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allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
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DP
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MQ
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ReadPosRankSum
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VQSLOD
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QD
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InbreedingCoeff
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FS
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SIO_000300: 0.0e0

MQRankSum
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BaseQRankSum
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SIO_000300: -7.27e-1

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 394
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50
num of homozygotes: 0

African
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allele count: 3
allele frequency: 3.554502369668246e-3
allele num: 844
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4832
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.324e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
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SIO_000300: 1.412e1

MQ
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.70863e5

ClippingRankSum
type: SiteQuality
SIO_000300: 3.31e-1

FS
type: SiteQuality
SIO_000300: 5.97e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.73e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.88e-1

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 46
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4726
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 236
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.228501228501228e-3
allele num: 814
num of homozygotes: 0

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

South Asian
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allele count: 3
allele frequency: 3.923620193565263e-4
allele num: 7646
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

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

ClippingRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 1
allele frequency: 1.30821559392988e-4
allele num: 7644
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
allele num: 152
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 768
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4682
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.62e1

FS
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MQ
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BaseQRankSum
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VQSLOD
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MQRankSum
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DP
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ClippingRankSum
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SIO_000300: 7.31e-1

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -8.98e-2

GenotypeQuality
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variant carriers: 1

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

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

European (Non-Finnish)
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allele count: 52
allele frequency: 1.129452649869679e-2
allele num: 4604
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African
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Latino
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allele num: 228
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East Asian
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South Asian
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allele count: 44
allele frequency: 5.762179151388162e-3
allele num: 7636
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Other
type: Population
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allele frequency: 1.948051948051948e-2
allele num: 154
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DP
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InbreedingCoeff
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FS
type: SiteQuality
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BaseQRankSum
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VQSLOD
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QD
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ClippingRankSum
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ReadPosRankSum
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MQ
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MQRankSum
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
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num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
allele num: 284
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Latino
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 150
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.299908003679853e-4
allele num: 4348
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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FS
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InbreedingCoeff
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DP
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QD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 2.305209774089442e-4
allele num: 4338
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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DP
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QD
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FS
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VQSLOD
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MQRankSum
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SIO_000300: -1.608e0

MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 3.47e0

InbreedingCoeff
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SIO_000300: -7.96e-2

ReadPosRankSum
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SIO_000300: 2.03e0

ClippingRankSum
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SIO_000300: -2.19e0

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

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

European (Finnish)
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 150
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African
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allele frequency: 0.0e0
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East Asian
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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FS
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MQ
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VQSLOD
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

Latino
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European (Non-Finnish)
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allele frequency: 1.417099669343411e-3
allele num: 4234
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South Asian
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allele frequency: 8.788037775445959e-3
allele num: 7624
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European (Finnish)
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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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East Asian
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QD
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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FS
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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MQ
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DP
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3872
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 612
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 5.250721974271463e-4
allele num: 7618
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Other
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BaseQRankSum
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MQRankSum
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FS
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MQ
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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QD
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 6.038330270412182e-3
allele num: 7618
num of homozygotes: 1

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: 0.0e0
allele num: 3872
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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FS
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ClippingRankSum
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ReadPosRankSum
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DP
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QD
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MQRankSum
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MQ
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VQSLOD
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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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GenotypeQuality
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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: NaN
allele num: 0
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Latino
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African
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South Asian
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European (Non-Finnish)
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Other
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East Asian
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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DP
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VQSLOD
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BaseQRankSum
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FS
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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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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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Latino
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Other
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European (Non-Finnish)
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East Asian
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ClippingRankSum
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ReadPosRankSum
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QD
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BaseQRankSum
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MQRankSum
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FS
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DP
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VQSLOD
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InbreedingCoeff
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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European (Finnish)
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Other
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DP
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.52e-1

FS
type: SiteQuality
SIO_000300: 3.212e0

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 8.36e-1

QD
type: SiteQuality
SIO_000300: 1.114e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.28e-1

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

GenotypeQuality
all individuals: 932
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 3

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

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2855
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 507
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 582
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 6.25e1
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 3
bin: 7.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1656
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3314
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 2.430555555555556e-2
allele num: 288
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 134
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.07e-2

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.62e-1

QD
type: SiteQuality
SIO_000300: 1.253e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.6007e4

VQSLOD
type: SiteQuality
SIO_000300: 4.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.45e-1

GenotypeQuality
all individuals: 77
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 690
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 9.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 219
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5266
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4196
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 815
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9052
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7206
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2210
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 654
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 912
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.808e1

MQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.3e-2

DP
type: SiteQuality
SIO_000300: 4.36378e5

VQSLOD
type: SiteQuality
SIO_000300: -1.095e0

GenotypeQuality
all individuals: 230
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2138
bin: 1.75e1
variant carriers: 10

GenotypeQuality
all individuals: 81
bin: 8.25e1
variant carriers: 5

GenotypeQuality
all individuals: 1216
bin: 6.75e1
variant carriers: 7

GenotypeQuality
all individuals: 77
bin: 5.75e1
variant carriers: 7

GenotypeQuality
all individuals: 2815
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 266
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5230
bin: 6.25e1
variant carriers: 10

GenotypeQuality
all individuals: 9364
bin: 2.25e1
variant carriers: 12

GenotypeQuality
all individuals: 596
bin: 2.75e1
variant carriers: 14

GenotypeQuality
all individuals: 28807
bin: 7.5e0
variant carriers: 10

GenotypeQuality
all individuals: 705
bin: 3.25e1
variant carriers: 5

GenotypeQuality
all individuals: 131
bin: 5.25e1
variant carriers: 7

GenotypeQuality
all individuals: 253
bin: 7.25e1
variant carriers: 8

GenotypeQuality
all individuals: 560
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 9.75e1
variant carriers: 141

GenotypeQuality
all individuals: 38
bin: 8.75e1
variant carriers: 14

GenotypeQuality
all individuals: 47
bin: 9.25e1
variant carriers: 16

South Asian
type: Population
allele count: 49
allele frequency: 6.681210799018271e-3
allele num: 7334
num of homozygotes: 2

African
type: Population
allele count: 4
allele frequency: 1.779359430604982e-3
allele num: 2248
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 6.122448979591836e-3
allele num: 490
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 940
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 80
allele frequency: 8.589220528237063e-3
allele num: 9314
num of homozygotes: 1

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

Other
type: Population
allele count: 4
allele frequency: 1.98019801980198e-2
allele num: 202
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.70207e5

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.95e-2

QD
type: SiteQuality
SIO_000300: 1.665e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

GenotypeQuality
all individuals: 66
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 435
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variant carriers: 0

GenotypeQuality
all individuals: 24415
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variant carriers: 0

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 1857
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variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
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variant carriers: 0

GenotypeQuality
all individuals: 1085
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2106
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6903
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
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variant carriers: 0

GenotypeQuality
all individuals: 18942
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 220
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7712
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 982
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 9.752291788570315e-5
allele num: 10254
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.42e-1

DP
type: SiteQuality
SIO_000300: 5.45308e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.32e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.41e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.011e0

QD
type: SiteQuality
SIO_000300: 8.369999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.61e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.875e0

GenotypeQuality
all individuals: 593
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2180
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variant carriers: 0

GenotypeQuality
all individuals: 373
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GenotypeQuality
all individuals: 55
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variant carriers: 0

GenotypeQuality
all individuals: 34
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GenotypeQuality
all individuals: 942
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variant carriers: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 22
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GenotypeQuality
all individuals: 290
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.259445843828715e-3
allele num: 794
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11862
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2572
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 234
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1126
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7990
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1032
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.509e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.43e-2

FS
type: SiteQuality
SIO_000300: 5.843e0

MQ
type: SiteQuality
SIO_000300: 6.178e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

VQSLOD
type: SiteQuality
SIO_000300: 1.12e-1

DP
type: SiteQuality
SIO_000300: 6.08216e5

ClippingRankSum
type: SiteQuality
SIO_000300: -7.2e-1

GenotypeQuality
all individuals: 25
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 893
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 7730
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 27390
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 101
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17528
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 74
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2343
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 30
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 76
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1545
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 7.25e1
variant carriers: 1

South Asian
type: Population
allele count: 1
allele frequency: 1.248751248751249e-4
allele num: 8008
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1040
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 236
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.225490196078431e-3
allele num: 816
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 3.469545104086353e-3
allele num: 2594
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1134
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12016
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.37e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1