4-74270797-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74270797
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74270797
    reference: chr 4
allele count: 2
allele frequency: 1.683501683501683e-5
allele num: 118800
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.80-36G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.121-36G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.49-36G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+674G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.121-41G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.80-36G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.80-36G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.86-36G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.80-36G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-102+674G>A
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2649
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5094
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11505
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31513
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1673
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5340
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

4-74270799-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74270799
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74270799
    reference: chr 4
allele count: 2
allele frequency: 1.678443746957821e-5
allele num: 119158
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.121-39A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.86-34A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.80-34A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.80-34A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.49-34A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.80-34A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.80-34A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.121-34A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-102+676A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+676A>G
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11629
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31790
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5093
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2644
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1729
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2233
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

4-74270810-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74270810
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74270811
    reference: chr 4
allele count: 4
allele frequency: 3.338953905741331e-5
allele num: 119798
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+695dupT
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.121-15dupT
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.80-15dupT
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.80-15dupT
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.121-20dupT
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.80-15dupT
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.86-15dupT
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.80-15dupT
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.49-15dupT
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-102+695dupT
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 12193
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31081
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5551
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1652
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff

4-74270810-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74270810
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74270809
    reference: chr 4
allele count: 2
allele frequency: 1.669476952870666e-5
allele num: 119798
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.80-15delT
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.121-15delT
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.49-15delT
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.86-15delT
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.80-15delT
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+695delT
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.80-15delT
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-102+695delT
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.121-20delT
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.80-15delT
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 12193
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5551
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31081
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 7.5e0
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: CT
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

4-74270818-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74270818
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74270818
    reference: chr 4
allele count: 6
allele frequency: 4.973722167879702e-5
allele num: 120634
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.80-15T>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-102+695T>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.80-15T>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+695T>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.80-15T>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.121-20T>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.80-15T>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.49-15T>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.121-15T>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.86-15T>A
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31420
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13008
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5410
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1744
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: T
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/4-74270819-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74270819
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74270819
    reference: chr 4
allele count: 2
allele frequency: 1.657330372236402e-5
allele num: 120676
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-102+696C>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.80-14C>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.86-14C>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.80-14C>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.121-14C>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.80-14C>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.49-14C>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.80-14C>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+696C>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.121-19C>A
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31411
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2668
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13020
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5428
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 741
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

4-74270822-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74270822
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74270822
    reference: chr 4
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.80-11C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.49-11C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.80-11C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-102+699C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.121-11C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.86-11C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.80-11C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+699C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.80-11C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.121-16C>T
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13081
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31466
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5414
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2664
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38974
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8095
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

4-74270830-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74270830
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74270830
    reference: chr 4
allele count: 2
allele frequency: 1.654369189028224e-5
allele num: 120892
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.80-3C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.121-3C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.80-3C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.49-3C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+707C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.86-3C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.80-3C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-102+707C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.80-3C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.121-8C>T
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5411
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13151
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31493
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2662
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
hgvs: c.80-3C>T
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD

4-74270839-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74270839
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74270839
    reference: chr 4
allele count: 1
allele frequency: 8.268289456277286e-6
allele num: 120944
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.55G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.92G>A
  hgvsp: ENSP00000392541.1:p.Ser31Asn
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.86G>A
  hgvsp: ENSP00000295897.4:p.Ser29Asn
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.86G>A
  hgvsp: ENSP00000401820.2:p.Ser29Asn
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.127G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.86G>A
  hgvsp: ENSP00000422784.1:p.Ser29Asn
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.86G>A
  hgvsp: ENSP00000384695.3:p.Ser29Asn
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.122G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+716G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-102+716G>A
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2661
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31495
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13188
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39135
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser29Asn
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

4-74270844-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74270844
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74270844
    reference: chr 4
allele count: 1
allele frequency: 8.268289456277286e-6
allele num: 120944
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.91G>A
  hgvsp: ENSP00000295897.4:p.Val31Ile
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.91G>A
  hgvsp: ENSP00000401820.2:p.Val31Ile
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.132G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.127G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-102+721G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.91G>A
  hgvsp: ENSP00000422784.1:p.Val31Ile
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+721G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.91G>A
  hgvsp: ENSP00000384695.3:p.Val31Ile
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.97G>A
  hgvsp: ENSP00000392541.1:p.Val33Ile
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.60G>A
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13201
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31469
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1656
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val31Ile
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

4-74270849-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74270849
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74270849
    reference: chr 4
allele count: 1
allele frequency: 8.269246671628215e-6
allele num: 120930
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.132T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+726T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-102+726T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.96T>C
  hgvsp: ENST00000415165.2:c.96T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.65T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.96T>C
  hgvsp: ENST00000509063.1:c.96T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.96T>C
  hgvsp: ENST00000401494.3:c.96T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.96T>C
  hgvsp: ENST00000295897.4:c.96T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.102T>C
  hgvsp: ENST00000441319.1:c.102T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.137T>C
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13232
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2661
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31426
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 740
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala32Ala
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/4-74270853-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74270853
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74270853
    reference: chr 4
allele count: 3
allele frequency: 2.481225394514838e-5
allele num: 120908
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.136C>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.100C>A
  hgvsp: ENST00000415165.2:c.100C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.106C>A
  hgvsp: ENST00000441319.1:c.106C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.100C>A
  hgvsp: ENST00000509063.1:c.100C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+730C>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.69C>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.100C>A
  hgvsp: ENST00000295897.4:c.100C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.141C>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-102+730C>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.100C>A
  hgvsp: ENST00000401494.3:c.100C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2662
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31392
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5635
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg34Arg
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

4-74270854-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74270854
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74270854
    reference: chr 4
allele count: 1
allele frequency: 8.271024945411235e-6
allele num: 120904
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.101G>A
  hgvsp: ENSP00000422784.1:p.Arg34Gln
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.137G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+731G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.70G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.107G>A
  hgvsp: ENSP00000392541.1:p.Arg36Gln
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-102+731G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.101G>A
  hgvsp: ENSP00000401820.2:p.Arg34Gln
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.101G>A
  hgvsp: ENSP00000384695.3:p.Arg34Gln
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.142G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.101G>A
  hgvsp: ENSP00000295897.4:p.Arg34Gln
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2662
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13247
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31375
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5630
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg34Gln
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

4-74270862-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74270862
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74270862
    reference: chr 4
allele count: 3
allele frequency: 2.48208760114507e-5
allele num: 120866
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.78G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.109G>A
  hgvsp: ENSP00000401820.2:p.Asp37Asn
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+739G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.109G>A
  hgvsp: ENSP00000422784.1:p.Asp37Asn
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.109G>A
  hgvsp: ENSP00000384695.3:p.Asp37Asn
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.109G>A
  hgvsp: ENSP00000295897.4:p.Asp37Asn
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-102+739G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.115G>A
  hgvsp: ENSP00000392541.1:p.Asp39Asn
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.150G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.145G>A
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31300
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5411
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13267
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2661
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1740
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asp37Asn
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

4-74270863-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74270863
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74270863
    reference: chr 4
allele count: 2
allele frequency: 1.654752449033625e-5
allele num: 120864
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-102+740A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.151A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.79A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.110A>G
  hgvsp: ENSP00000422784.1:p.Asp37Gly
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.110A>G
  hgvsp: ENSP00000401820.2:p.Asp37Gly
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.110A>G
  hgvsp: ENSP00000384695.3:p.Asp37Gly
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.116A>G
  hgvsp: ENSP00000392541.1:p.Asp39Gly
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+740A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.110A>G
  hgvsp: ENSP00000295897.4:p.Asp37Gly
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.146A>G
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31296
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13272
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5406
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 39005
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp37Gly
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

4-74270864-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74270864
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74270864
    reference: chr 4
allele count: 6
allele frequency: 4.964257347100873e-5
allele num: 120864
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.147T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+741T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-102+741T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.111T>C
  hgvsp: ENST00000295897.4:c.111T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.111T>C
  hgvsp: ENST00000509063.1:c.111T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.117T>C
  hgvsp: ENST00000441319.1:c.117T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.111T>C
  hgvsp: ENST00000415165.2:c.111T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.111T>C
  hgvsp: ENST00000401494.3:c.111T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.80T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.152T>C
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31288
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13268
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2663
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp37Asp
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/4-74270878-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74270878
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74270878
    reference: chr 4
allele count: 2
allele frequency: 1.657247974014352e-5
allele num: 120682
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.94A>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.125A>C
  hgvsp: ENSP00000422784.1:p.Asn42Thr
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.131A>C
  hgvsp: ENSP00000392541.1:p.Asn44Thr
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.125A>C
  hgvsp: ENSP00000401820.2:p.Asn42Thr
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.125A>C
  hgvsp: ENSP00000295897.4:p.Asn42Thr
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+755A>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-102+755A>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.166A>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.125A>C
  hgvsp: ENSP00000384695.3:p.Asn42Thr
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.161A>C
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31048
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2658
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn42Thr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD

4-74270878-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74270878
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74270877
    reference: chr 4
allele count: 1
allele frequency: 8.286239870071759e-6
allele num: 120682
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.128delT
  hgvsp: ENSP00000422784.1:p.Phe43SerfsTer6
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.97delT
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.128delT
  hgvsp: ENSP00000384695.3:p.Phe43SerfsTer83
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.128delT
  hgvsp: ENSP00000295897.4:p.Phe43SerfsTer6
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.169delT
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.128delT
  hgvsp: ENSP00000401820.2:p.Phe43SerfsTer6
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.134delT
  hgvsp: ENSP00000392541.1:p.Phe45SerfsTer6
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.164delT
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+758delT
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-102+758delT
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31048
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2658
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2216
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Phe43SerfsTer6
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: AT
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

4-74270909-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74270909
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74270909
    reference: chr 4
allele count: 5
allele frequency: 4.19702514857469e-5
allele num: 119132
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.137+19G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.173+19G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.106+19G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.143+19G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+786G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+19G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+19G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.137+19G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-102+786G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.178+19G>A
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12469
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26240
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5231
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3867
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2185
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32951
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

4-74270918-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74270918
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74270918
    reference: chr 4
allele count: 2
allele frequency: 1.687279599102367e-5
allele num: 118534
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+795T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.143+28T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.137+28T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.178+28T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.173+28T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.137+28T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.106+28T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+28T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+28T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-102+795T>G
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11424
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6638
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4562
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4440
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

4-74270927-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74270927
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74270927
    reference: chr 4
allele count: 36
allele frequency: 3.056079050578108e-4
allele num: 117798
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.173+37C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+37C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-102+804C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.178+37C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+37C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.106+37C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.137+37C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.137+37C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.143+37C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+804C>G
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16287
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9244
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7647
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4978
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10633
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20416
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2130
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD

4-74270928-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74270928
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74270928
    reference: chr 4
allele count: 1
allele frequency: 8.497620666213461e-6
allele num: 117680
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+805T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+38T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.143+38T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.106+38T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.137+38T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.173+38T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+38T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.178+38T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-102+805T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.137+38T>G
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15752
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7663
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2651
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9919
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4930
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1576
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4671
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4329
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

4-74270942-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74270942
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74270942
    reference: chr 4
allele count: 1
allele frequency: 8.703826201998399e-6
allele num: 114892
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+819A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.137+52A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+52A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.106+52A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.173+52A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.178+52A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+52A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.137+52A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-102+819A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.143+52A>G
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7434
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11885
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15201
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4391
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2602
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2585
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1111
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1256
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/4-74272304-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272304
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272304
    reference: chr 4
allele count: 1
allele frequency: 8.446088616361763e-6
allele num: 118398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.107-42A>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.138-42A>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.144-42A>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.179-42A>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1414A>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1414A>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-101-42A>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.174-42A>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2181A>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.138-42A>C
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18737
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5913
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5732
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10344
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1013
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1793
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS

4-74272311-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272311
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272311
    reference: chr 4
allele count: 1
allele frequency: 8.42715566641947e-6
allele num: 118664
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.107-35T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2188T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1421T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.138-35T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-101-35T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1421T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.138-35T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.179-35T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.174-35T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.144-35T>C
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3333
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22934
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4623
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2070
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6392
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1450
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum

4-74272317-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272317
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272317
    reference: chr 4
allele count: 1
allele frequency: 8.403078888104602e-6
allele num: 119004
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-101-29A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.138-29A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1427A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.138-29A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1427A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2194A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.179-29A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.107-29A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.174-29A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.144-29A>G
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6071
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1784
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2847
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11500
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25597
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1151
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

4-74272321-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272321
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272321
    reference: chr 4
allele count: 1
allele frequency: 8.375770570892522e-6
allele num: 119392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2198C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.179-25C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.107-25C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.144-25C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.138-25C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.138-25C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1431C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.174-25C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1431C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-101-25C>T
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26184
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6167
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11985
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6655
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

4-74272330-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272330
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272330
    reference: chr 4
allele count: 2
allele frequency: 1.664807631478183e-5
allele num: 120134
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.144-16A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.138-16A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.107-16A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-101-16A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.179-16A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1440A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2207A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.138-16A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1440A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.174-16A>G
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12463
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27865
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3363
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2159
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

4-74272335-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272335
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272335
    reference: chr 4
allele count: 1
allele frequency: 8.304268393954492e-6
allele num: 120420
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1445C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.107-11C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.138-11C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2212C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.174-11C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1445C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-101-11C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.138-11C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.144-11C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.179-11C>T
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3371
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12704
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6349
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2164
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD

4-74272340-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272340
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272340
    reference: chr 4
allele count: 1
allele frequency: 8.288849839196314e-6
allele num: 120644
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.138-6T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.138-6T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.174-6T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-101-6T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.107-6T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2217T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1450T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.144-6T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.179-6T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1450T>C
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3365
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6352
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2166
  bin: 8.25e1
  variant carriers: 0
hgvs: c.138-6T>C
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP

4-74272343-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272343
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272343
    reference: chr 4
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.138-3C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.138-3C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.107-3C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.144-3C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.174-3C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1453C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-101-3C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2220C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.179-3C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1453C>T
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28324
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12923
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2311
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3372
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6983
  bin: 6.75e1
  variant carriers: 0
hgvs: c.138-3C>T
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

4-74272347-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272347
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272347
    reference: chr 4
allele count: 1
allele frequency: 8.271024945411235e-6
allele num: 120904
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.145G>A
  hgvsp: ENSP00000392541.1:p.Val49Met
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-100G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.139G>A
  hgvsp: ENSP00000295897.4:p.Val47Met
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.108G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.175G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1457G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.139G>A
  hgvsp: ENSP00000422784.1:p.Val47Met
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.180G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1457G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2224G>A
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3375
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28304
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6389
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2306
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13059
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val47Met
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-74272349-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272349
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272349
    reference: chr 4
allele count: 1
allele frequency: 8.267742575567167e-6
allele num: 120952
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.110G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-98G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1459G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2226G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.147G>A
  hgvsp: ENST00000441319.1:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.182G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.141G>A
  hgvsp: ENST00000509063.1:c.141G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.141G>A
  hgvsp: ENST00000295897.4:c.141G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1459G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.177G>A
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28264
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13125
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6399
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3376
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1418
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Val47Val
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

4-74272368-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272368
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272368
    reference: chr 4
allele count: 1
allele frequency: 8.253685270473266e-6
allele num: 121158
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-79T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.196T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1478T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.166T>C
  hgvsp: ENSP00000392541.1:p.Tyr56His
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.201T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.160T>C
  hgvsp: ENSP00000422784.1:p.Tyr54His
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1478T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.129T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.160T>C
  hgvsp: ENSP00000295897.4:p.Tyr54His
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2245T>C
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6425
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3371
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1416
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Tyr54His
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum

4-74272392-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272392
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272392
    reference: chr 4
allele count: 2
allele frequency: 1.650056101907465e-5
allele num: 121208
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.220G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.153G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.184G>A
  hgvsp: ENSP00000295897.4:p.Asp62Asn
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.184G>A
  hgvsp: ENSP00000422784.1:p.Asp62Asn
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-55G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1502G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.190G>A
  hgvsp: ENSP00000392541.1:p.Asp64Asn
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2269G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.225G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1502G>A
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27765
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6457
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3377
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp62Asn
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

4-74272399-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272399
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272399
    reference: chr 4
allele count: 1
allele frequency: 8.25000825000825e-6
allele num: 121212
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1509T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.227T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.191T>C
  hgvsp: ENSP00000422784.1:p.Val64Ala
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2276T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-48T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.191T>C
  hgvsp: ENSP00000295897.4:p.Val64Ala
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1509T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.232T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.160T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.197T>C
  hgvsp: ENSP00000392541.1:p.Val66Ala
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13666
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6451
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2314
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 895
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7085
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val64Ala
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

4-74272416-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272416
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272416
    reference: chr 4
allele count: 6
allele frequency: 4.949841605068638e-5
allele num: 121216
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.208G>A
  hgvsp: ENSP00000422784.1:p.Val70Ile
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-31G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1526G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.208G>A
  hgvsp: ENSP00000295897.4:p.Val70Ile
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2293G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1526G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.177G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.214G>A
  hgvsp: ENSP00000392541.1:p.Val72Ile
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.249G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.244G>A
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3374
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6449
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2311
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27491
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13796
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36040
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Val70Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD

4-74272431-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272431
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272431
    reference: chr 4
allele count: 1
allele frequency: 8.248239000973292e-6
allele num: 121238
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.264A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.223A>G
  hgvsp: ENSP00000295897.4:p.Lys75Glu
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.223A>G
  hgvsp: ENSP00000422784.1:p.Lys75Glu
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-16A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.259A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1541A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.229A>G
  hgvsp: ENSP00000392541.1:p.Lys77Glu
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2308A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1541A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.192A>G
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13917
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27395
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3376
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6452
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2206
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Lys75Glu
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

4-74272435-CAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272435
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272433
    reference: chr 4
allele count: 7
allele frequency: 5.773481574345947e-5
allele num: 121244
alternate allele: C
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.197_198delAT
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1546_137+1547delAT
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: frameshift_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.228_229delAT
  hgvsp: ENSP00000422784.1:p.Val78CysfsTer2
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.269_270delAT
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  clinical significance: not_provided
  consequence: frameshift_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.228_229delAT
  hgvsp: ENSP00000295897.4:p.Val78CysfsTer2
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.264_265delAT
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: frameshift_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.234_235delAT
  hgvsp: ENSP00000392541.1:p.Val80CysfsTer2
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-11_-10delAT
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1546_137+1547delAT
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2313_79+2314delAT
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13915
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3377
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val78CysfsTer2
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: CAT
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

4-74272439-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272439
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272439
    reference: chr 4
allele count: 1
allele frequency: 8.24783082049421e-6
allele num: 121244
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1549T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1549T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2316T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.237T>C
  hgvsp: ENST00000441319.1:c.237T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.-8T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.272T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.231T>C
  hgvsp: ENST00000509063.1:c.231T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.231T>C
  hgvsp: ENST00000295897.4:c.231T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.267T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.200T>C
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3377
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6466
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27334
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1784
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13968
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Cys77Cys
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

4-74272456-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272456
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272456
    reference: chr 4
allele count: 58
allele frequency: 4.785320616481304e-4
allele num: 121204
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.254C>T
  hgvsp: ENSP00000392541.1:p.Ala85Val
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.248C>T
  hgvsp: ENSP00000422784.1:p.Ala83Val
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.248C>T
  hgvsp: ENSP00000295897.4:p.Ala83Val
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.284C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2333C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1566C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.217C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1566C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.10C>T
  hgvsp: ENST00000503124.1:c.10C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.289C>T
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3383
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27138
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2311
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14064
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6482
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 3.75e1
  variant carriers: 1
hgvs: p.Ala83Val
num of homozygotes: 3
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

4-74272456-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272456
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272456
    reference: chr 4
allele count: 2
allele frequency: 1.650110557407346e-5
allele num: 121204
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.10C>G
  hgvsp: ENSP00000421027.1:p.Leu4Val
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.248C>G
  hgvsp: ENSP00000422784.1:p.Ala83Gly
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.284C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1566C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.254C>G
  hgvsp: ENSP00000392541.1:p.Ala85Gly
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.248C>G
  hgvsp: ENSP00000295897.4:p.Ala83Gly
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.289C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1566C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.217C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2333C>G
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14064
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2311
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3383
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6482
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36050
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala83Gly
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/4-74272475-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272475
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272475
    reference: chr 4
allele count: 1
allele frequency: 8.256547442121603e-6
allele num: 121116
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.267A>C
  hgvsp: ENST00000509063.1:c.267A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.267A>C
  hgvsp: ENST00000295897.4:c.267A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.308A>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.273A>C
  hgvsp: ENST00000441319.1:c.273A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1585A>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.29A>C
  hgvsp: ENSP00000421027.1:p.His10Pro
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.236A>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.303A>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2352A>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1585A>C
  variant of: http://identifiers.org/hgnc/399
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6481
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26873
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2311
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14130
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3372
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2185
  bin: 7.25e1
  variant carriers: 0
hgvs: p.His10Pro
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD

4-74272476-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272476
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272476
    reference: chr 4
allele count: 2
allele frequency: 1.651473114017704e-5
allele num: 121104
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.30C>G
  hgvsp: ENSP00000421027.1:p.His10Gln
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1586C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.274C>G
  hgvsp: ENSP00000392541.1:p.Leu92Val
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.268C>G
  hgvsp: ENSP00000422784.1:p.Leu90Val
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.237C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2353C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.304C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.268C>G
  hgvsp: ENSP00000295897.4:p.Leu90Val
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.309C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1586C>G
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1784
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26849
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2314
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14138
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3375
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu90Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/4-74272485-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272485
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272485
    reference: chr 4
allele count: 1
allele frequency: 8.258865892535638e-6
allele num: 121082
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.239+7A>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.311+7A>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.270+7A>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.276+7A>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1595A>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.306+7A>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2362A>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.32+7A>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.270+7A>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1595A>C
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3370
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1784
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1419
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7242
  bin: 9.75e1
  variant carriers: 1
hgvs: c.270+7A>C
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

4-74272486-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272486
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272486
    reference: chr 4
allele count: 1
allele frequency: 8.260366760284156e-6
allele num: 121060
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.239+8C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.270+8C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.270+8C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1596C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.32+8C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.311+8C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2363C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.276+8C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.306+8C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1596C>T
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26540
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3373
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1418
  bin: 9.25e1
  variant carriers: 0
hgvs: c.270+8C>T
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

4-74272487-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272487
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272487
    reference: chr 4
allele count: 1
allele frequency: 8.260366760284156e-6
allele num: 121060
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1597A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.270+9A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1597A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.270+9A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.276+9A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.311+9A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.32+9A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.239+9A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.306+9A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2364A>G
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26491
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3369
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14035
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 885
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

4-74272490-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272490
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272490
    reference: chr 4
allele count: 1
allele frequency: 8.26255081468751e-6
allele num: 121028
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1600C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1600C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.32+12C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.239+12C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.306+12C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.311+12C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.276+12C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2367C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.270+12C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.270+12C>G
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6433
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13981
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2315
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26306
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3375
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 650
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/4-74272505-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272505
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272505
    reference: chr 4
allele count: 1
allele frequency: 8.268973158913126e-6
allele num: 120934
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1615C>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.239+27C>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1615C>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2382C>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.306+27C>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.270+27C>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.276+27C>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.270+27C>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.32+27C>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.311+27C>A
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13507
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24441
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1784
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1386
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2788
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: C
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

4-74272505-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272505
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272505
    reference: chr 4
allele count: 1
allele frequency: 8.268973158913126e-6
allele num: 120934
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.311+27C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.32+27C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1615C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.270+27C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1615C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.276+27C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.270+27C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.239+27C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2382C>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.306+27C>G
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13507
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1784
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24441
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 944
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

4-74272506-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272506
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272506
    reference: chr 4
allele count: 1
allele frequency: 8.268289456277286e-6
allele num: 120944
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.311+28T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.270+28T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1616T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.32+28T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2383T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.270+28T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.276+28T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1616T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.239+28T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.306+28T>C
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6331
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23907
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1554
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2142
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff

4-74272511-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272511
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272510
    reference: chr 4
allele count: 1
allele frequency: 8.269520202437855e-6
allele num: 120926
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.306+34delC
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1622delC
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.276+34delC
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1622delC
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.239+34delC
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.311+34delC
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.32+34delC
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2389delC
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.270+34delC
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.270+34delC
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3357
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13160
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1055
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2768
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
reference allele: TC
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum

4-74272515-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272515
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272515
    reference: chr 4
allele count: 90
allele frequency: 7.44774167921749e-4
allele num: 120842
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.270+37T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.239+37T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2392T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1625T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.276+37T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1625T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.32+37T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.270+37T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.306+37T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.311+37T>C
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 21919
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12757
  bin: 2.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2318
  bin: 4.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 4784
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6248
  bin: 3.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3356
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1990
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

4-74272530-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74272530
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74272530
    reference: chr 4
allele count: 1
allele frequency: 8.37058242512514e-6
allele num: 119466
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.137+1640A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.306+52A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.311+52A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.276+52A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.79+2407A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.239+52A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.32+52A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.270+52A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+1640A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.270+52A>G
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3465
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14110
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7302
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1726
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11223
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum

4-74274276-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74274276
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74274276
    reference: chr 4
allele count: 3
allele frequency: 2.940369310385384e-5
allele num: 102028
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.277-35T>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.271-35T>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+3386T>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.138-796T>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.240-35T>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.271-35T>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.312-35T>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.80-796T>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.307-35T>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.33-796T>A
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9022
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2897
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13728
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3738
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1553
  bin: 4.25e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD

4-74274276-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74274276
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74274276
    reference: chr 4
allele count: 1
allele frequency: 9.801231034617949e-6
allele num: 102028
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.307-35T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.240-35T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.271-35T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.138-796T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.33-796T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+3386T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.312-35T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.277-35T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.80-796T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.271-35T>G
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2897
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13728
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9022
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4616
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9238
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

4-74274284-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74274284
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74274284
    reference: chr 4
allele count: 1
allele frequency: 9.425248355294162e-6
allele num: 106098
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.312-27A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.240-27A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.277-27A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.138-788A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.307-27A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.80-788A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+3394A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.271-27A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.271-27A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.33-788A>G
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7592
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7315
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3080
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29069
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

4-74274285-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74274285
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74274285
    reference: chr 4
allele count: 5
allele frequency: 4.690343520759461e-5
allele num: 106602
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.271-26A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.277-26A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.138-787A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.33-787A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.307-26A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.271-26A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.312-26A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.80-787A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.137+3395A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.240-26A>G
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7034
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9082
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 29916
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
reference allele: A
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

4-74274303-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74274303
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74274303
    reference: chr 4
allele count: 1418
allele frequency: 1.235772924546389e-2
allele num: 114746
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.80-769C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.138-3410C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.271-8C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.277-8C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.33-769C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.240-8C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.271-8C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.307-8C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.312-8C>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.138-769C>T
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 5.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 1.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 3.25e1
  variant carriers: 232
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 4.75e1
  variant carriers: 93
genotype depth: GenotypeDepth
  all individuals: 11161
  bin: 2.75e1
  variant carriers: 202
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 1.75e1
  variant carriers: 93
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 4.25e1
  variant carriers: 128
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.25e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 3.75e1
  variant carriers: 162
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.75e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 37229
  bin: 2.25e1
  variant carriers: 193
genotype quality: GenotypeQuality
  all individuals: 736
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 4.75e1
  variant carriers: 2
hgvs: c.271-8C>T
num of homozygotes: 9
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

4-74274305-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74274305
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74274305
    reference: chr 4
allele count: 2
allele frequency: 1.730852444829078e-5
allele num: 115550
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.312-6A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.240-6A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.138-3408A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.271-6A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.80-767A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.277-6A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.33-767A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.271-6A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.307-6A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.138-767A>G
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3496
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37841
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11882
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1363
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 2.75e1
  variant carriers: 0
hgvs: c.271-6A>G
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS

4-74274312-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74274312
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74274312
    reference: chr 4
allele count: 2
allele frequency: 1.702533369654045e-5
allele num: 117472
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.272A>G
  hgvsp: ENSP00000295897.4:p.His91Arg
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.138-3401A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.272A>G
  hgvsp: ENSP00000422784.1:p.His91Arg
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.241A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.278A>G
  hgvsp: ENSP00000392541.1:p.His93Arg
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.33-760A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.80-760A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.138-760A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.313A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.308A>G
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38946
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12363
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3544
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 3.25e1
  variant carriers: 0
hgvs: p.His91Arg
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/4-74274315-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74274315
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74274315
    reference: chr 4
allele count: 1
allele frequency: 8.481908090043937e-6
allele num: 117898
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.281C>A
  hgvsp: ENSP00000392541.1:p.Thr94Asn
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.80-757C>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.244C>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.316C>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.138-757C>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.311C>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.275C>A
  hgvsp: ENSP00000422784.1:p.Thr92Asn
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.275C>A
  hgvsp: ENSP00000295897.4:p.Thr92Asn
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.138-3398C>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.33-757C>A
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3600
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39134
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12472
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1361
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr92Asn
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ

4-74274322-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74274322
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74274322
    reference: chr 4
allele count: 1
allele frequency: 8.416374899003501e-6
allele num: 118816
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.33-750T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.251T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.282T>C
  hgvsp: ENST00000295897.4:c.282T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.323T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.138-750T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.318T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.138-3391T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.80-750T>C
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.288T>C
  hgvsp: ENST00000441319.1:c.288T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.282T>C
  hgvsp: ENST00000509063.1:c.282T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12874
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 846
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1360
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Phe94Phe
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

4-74274338-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74274338
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74274338
    reference: chr 4
allele count: 1
allele frequency: 8.337224037884346e-6
allele num: 119944
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.339A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.298A>G
  hgvsp: ENSP00000295897.4:p.Thr100Ala
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.138-3375A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.138-734A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.267A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.304A>G
  hgvsp: ENSP00000392541.1:p.Thr102Ala
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.33-734A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.80-734A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.298A>G
  hgvsp: ENSP00000422784.1:p.Thr100Ala
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.334A>G
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39656
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3709
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 808
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr100Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

4-74274351-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74274351
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74274351
    reference: chr 4
allele count: 1
allele frequency: 8.30923654734603e-6
allele num: 120348
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.311T>G
  hgvsp: ENSP00000295897.4:p.Leu104Arg
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.80-721T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.138-3362T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.347T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.317T>G
  hgvsp: ENSP00000392541.1:p.Leu106Arg
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.280T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.311T>G
  hgvsp: ENSP00000422784.1:p.Leu104Arg
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.352T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.33-721T>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.138-721T>G
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13730
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3719
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 984
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Leu104Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: FS

4-74274354-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74274354
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74274354
    reference: chr 4
allele count: 1
allele frequency: 8.304820117596252e-6
allele num: 120412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.138-718G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.80-718G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.350G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.355G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.283G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.33-718G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.138-3359G>A
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.314G>A
  hgvsp: ENSP00000295897.4:p.Arg105His
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.320G>A
  hgvsp: ENSP00000392541.1:p.Arg107His
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.314G>A
  hgvsp: ENSP00000422784.1:p.Arg105His
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3764
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13801
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39456
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 872
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg105His
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

4-74274363-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74274363
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74274363
    reference: chr 4
allele count: 53
allele frequency: 4.39534922293543e-4
allele num: 120582
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.323A>G
  hgvsp: ENSP00000295897.4:p.Tyr108Cys
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.359A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000505649
  gene symbol: ALB
  hgvsc: ENST00000505649.1:n.9A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.33-709A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.138-3350A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.329A>G
  hgvsp: ENSP00000392541.1:p.Tyr110Cys
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.323A>G
  hgvsp: ENSP00000422784.1:p.Tyr108Cys
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.138-709A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.80-709A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.364A>G
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.292A>G
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3752
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39326
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 13921
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Tyr108Cys
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ

4-74274365-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74274365
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74274365
    reference: chr 4
allele count: 1
allele frequency: 8.292699107705576e-6
allele num: 120588
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.33-707G>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.366G>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.361G>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.325G>T
  hgvsp: ENSP00000295897.4:p.Gly109Cys
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.331G>T
  hgvsp: ENSP00000392541.1:p.Gly111Cys
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.294G>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.325G>T
  hgvsp: ENSP00000422784.1:p.Gly109Cys
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.138-707G>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000505649
  gene symbol: ALB
  hgvsc: ENST00000505649.1:n.11G>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.80-707G>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.138-3348G>T
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39311
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13968
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3772
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly109Cys
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
reference allele: G
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

4-74274370-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74274370
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 74274370
    reference: chr 4
allele count: 1
allele frequency: 8.288849839196314e-6
allele num: 120644
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000510166
  gene symbol: ALB
  hgvsc: ENST00000510166.1:n.366A>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000392541
  ensembl transcript: ENST00000441319
  gene symbol: ALB
  hgvsc: ENST00000441319.1:c.336A>T
  hgvsp: ENSP00000392541.1:p.Glu112Asp
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000505649
  gene symbol: ALB
  hgvsc: ENST00000505649.1:n.16A>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000514786
  gene symbol: ALB
  hgvsc: ENST00000514786.1:n.299A>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000295897
  ensembl transcript: ENST00000295897
  gene symbol: ALB
  hgvsc: ENST00000295897.4:c.330A>T
  hgvsp: ENSP00000295897.4:p.Glu110Asp
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000422784
  ensembl transcript: ENST00000509063
  gene symbol: ALB
  hgvsc: ENST00000509063.1:c.330A>T
  hgvsp: ENSP00000422784.1:p.Glu110Asp
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000423727
  ensembl transcript: ENST00000476441
  gene symbol: ALB
  hgvsc: ENST00000476441.2:c.80-702A>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000384695
  ensembl transcript: ENST00000401494
  gene symbol: ALB
  hgvsc: ENST00000401494.3:c.138-702A>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163631
  ensembl transcript: ENST00000515133
  gene symbol: ALB
  hgvsc: ENST00000515133.1:n.371A>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000421027
  ensembl transcript: ENST00000503124
  gene symbol: ALB
  hgvsc: ENST00000503124.1:c.33-702A>T
  variant of: http://identifiers.org/hgnc/399
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163631
  ensembl protein: ENSP00000401820
  ensembl transcript: ENST00000415165
  gene symbol: ALB
  hgvsc: ENST00000415165.2:c.138-3343A>T
  variant of: http://identifiers.org/hgnc/399
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39199
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14065
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Glu110Asp
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 83
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8098
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1719
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37102
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1268
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2223
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1122
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9810
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.056701818737582e-5
allele num: 65430
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16190
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.841427e6

FS
type: SiteQuality
SIO_000300: 8.618e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.429e0

VQSLOD
type: SiteQuality
SIO_000300: -2.296e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.936e1

MQRankSum
type: SiteQuality
SIO_000300: 5.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.32e-1

QD
type: SiteQuality
SIO_000300: 1.505e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.83e-1

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523043650431021e-5
allele num: 65658
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16234
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11416
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.017915309446254e-4
allele num: 9824
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8546
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.95e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 9.88e-1

DP
type: SiteQuality
SIO_000300: 1.846467e6

QD
type: SiteQuality
SIO_000300: 1.443e1

VQSLOD
type: SiteQuality
SIO_000300: 7.84e-1

FS
type: SiteQuality
SIO_000300: 1.793e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.59e-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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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.028192471913515e-5
allele num: 66046
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.716875871687587e-5
allele num: 11472
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.132711885195633e-5
allele num: 16306
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9914
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.882408e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.149e0

MQRankSum
type: SiteQuality
SIO_000300: -9.0e-2

QD
type: SiteQuality
SIO_000300: 4.75e0

VQSLOD
type: SiteQuality
SIO_000300: 7.69e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.5e-2

FS
type: SiteQuality
SIO_000300: 5.631e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9914
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.132711885195633e-5
allele num: 16306
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514096235956757e-5
allele num: 66046
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 7.69e-1

DP
type: SiteQuality
SIO_000300: 1.882408e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.88e-1

QD
type: SiteQuality
SIO_000300: 4.75e0

MQRankSum
type: SiteQuality
SIO_000300: -9.0e-2

FS
type: SiteQuality
SIO_000300: 5.631e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.149e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.5e-2

MQ
type: SiteQuality
SIO_000300: 5.961e1

GenotypeQuality
all individuals: 1120
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variant carriers: 0

GenotypeQuality
all individuals: 43
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9
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GenotypeQuality
all individuals: 26
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.013409904086112e-5
allele num: 66518
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.319647413593134e-4
allele num: 8622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10014
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.873712e6

QD
type: SiteQuality
SIO_000300: 1.392e1

VQSLOD
type: SiteQuality
SIO_000300: 3.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.45e-1

FS
type: SiteQuality
SIO_000300: 2.022e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.0e-2

MQ
type: SiteQuality
SIO_000300: 5.92e1

MQRankSum
type: SiteQuality
SIO_000300: 3.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.37e-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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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66540
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16432
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10024
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.319647413593134e-4
allele num: 8622
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
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MQRankSum
type: SiteQuality
SIO_000300: -6.6e-1

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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DP
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BaseQRankSum
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SIO_000300: -2.842e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 1.2843e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.17e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-2

GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502087902184036e-5
allele num: 66574
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
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QD
type: SiteQuality
SIO_000300: 1.055e1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.899e1

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
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DP
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SIO_000300: 1.875405e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.002822653294096e-5
allele num: 66604
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 904
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East Asian
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
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allele num: 10084
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.94e-1

ReadPosRankSum
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MQ
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InbreedingCoeff
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MQRankSum
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VQSLOD
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ClippingRankSum
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FS
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DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.154e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

Other
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
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African
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allele count: 1
allele frequency: 9.895111814763506e-5
allele num: 10106
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Latino
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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DP
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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QD
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FS
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MQ
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MQRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.50105073551486e-5
allele num: 66620
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6612
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Latino
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Other
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InbreedingCoeff
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FS
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QD
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ReadPosRankSum
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MQ
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.501095799933952e-5
allele num: 66618
num of homozygotes: 0

Other
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allele num: 904
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Latino
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allele frequency: 0.0e0
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East Asian
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South Asian
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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DP
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MQ
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SIO_000300: 6.0e1

MQRankSum
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FS
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.910802775024777e-5
allele num: 10090
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Other
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6610
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East Asian
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.002552169343942e-5
allele num: 66610
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DP
type: SiteQuality
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FS
type: SiteQuality
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QD
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -7.53e-1

MQRankSum
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MQ
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VQSLOD
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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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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

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

Other
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East Asian
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allele frequency: 0.0e0
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South Asian
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European (Non-Finnish)
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ClippingRankSum
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DP
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InbreedingCoeff
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MQ
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MQRankSum
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ReadPosRankSum
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FS
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QD
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VQSLOD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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European (Non-Finnish)
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South Asian
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African
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Latino
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Other
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MQRankSum
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FS
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DP
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ReadPosRankSum
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ClippingRankSum
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QD
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InbreedingCoeff
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VQSLOD
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MQ
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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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European (Finnish)
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African
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Latino
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South Asian
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East Asian
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Other
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European (Non-Finnish)
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DP
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QD
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FS
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VQSLOD
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ClippingRankSum
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MQ
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BaseQRankSum
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MQRankSum
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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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South Asian
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Other
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European (Finnish)
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East Asian
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Latino
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African
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European (Non-Finnish)
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VQSLOD
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MQ
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FS
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QD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

South Asian
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allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66510
num of homozygotes: 0

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

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

African
type: Population
allele count: 2
allele frequency: 1.995211492418196e-4
allele num: 10024
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.32e0

FS
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MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.49e-1

DP
type: SiteQuality
SIO_000300: 1.874495e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.122e1

MQ
type: SiteQuality
SIO_000300: 5.919e1

VQSLOD
type: SiteQuality
SIO_000300: 2.07e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10024
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503533303262667e-5
allele num: 66510
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.919e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.49e-1

InbreedingCoeff
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MQRankSum
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VQSLOD
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FS
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SIO_000300: 2.86e0

BaseQRankSum
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QD
type: SiteQuality
SIO_000300: 1.122e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.94e-1

DP
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SIO_000300: 1.874495e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5

Other
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allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16338
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 7.641287404101843e-5
allele num: 65434
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.78e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.6e-1

InbreedingCoeff
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VQSLOD
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FS
type: SiteQuality
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MQ
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DP
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BaseQRankSum
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QD
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.96e-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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bin: 4.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11420
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8524
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16282
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9782
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.074652564260239e-5
allele num: 65048
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.1e-2

QD
type: SiteQuality
SIO_000300: 1.697e1

MQRankSum
type: SiteQuality
SIO_000300: 9.429999999999999e-1

FS
type: SiteQuality
SIO_000300: 3.512e0

MQ
type: SiteQuality
SIO_000300: 5.911e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

DP
type: SiteQuality
SIO_000300: 1.766118e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.1e0

VQSLOD
type: SiteQuality
SIO_000300: -7.291e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e0

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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variant carriers: 0

Latino
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allele count: 3
allele frequency: 2.635277582572031e-4
allele num: 11384
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8444
num of homozygotes: 0

African
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allele count: 33
allele frequency: 3.39715873996294e-3
allele num: 9714
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16218
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64568
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

DP
type: SiteQuality
SIO_000300: 1.72655e6

ClippingRankSum
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MQRankSum
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FS
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BaseQRankSum
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.956e1

VQSLOD
type: SiteQuality
SIO_000300: 2.82e0

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9694
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.550243388211949e-5
allele num: 64506
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 4.792e1

FS
type: SiteQuality
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ClippingRankSum
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SIO_000300: 2.74e-1

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

Latino
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allele frequency: 0.0e0
allele num: 11198
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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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: 1
allele frequency: 1.598056762976221e-5
allele num: 62576
num of homozygotes: 0

MQRankSum
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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QD
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FS
type: SiteQuality
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VQSLOD
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MQ
type: SiteQuality
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 1
allele frequency: 6.180469715698394e-5
allele num: 16180
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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African
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64794
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Other
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MQRankSum
type: SiteQuality
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BaseQRankSum
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QD
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MQ
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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DP
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10184
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.53907716932927e-5
allele num: 64974
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.64e-1

VQSLOD
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InbreedingCoeff
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SIO_000300: 1.1e-3

MQRankSum
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FS
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QD
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ClippingRankSum
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DP
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MQ
type: SiteQuality
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BaseQRankSum
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SIO_000300: 4.06e0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10198
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
allele num: 16236
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11380
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.533695285420693e-5
allele num: 65202
num of homozygotes: 0

QD
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BaseQRankSum
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ReadPosRankSum
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DP
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VQSLOD
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MQ
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InbreedingCoeff
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SIO_000300: 5.999999999999999e-4

MQRankSum
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SIO_000300: 1.58e-1

FS
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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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South Asian
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allele frequency: 0.0e0
allele num: 16278
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10222
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Latino
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allele count: 1
allele frequency: 8.765778401122019e-5
allele num: 11408
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65452
num of homozygotes: 0

BaseQRankSum
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SIO_000300: -3.245e0

InbreedingCoeff
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SIO_000300: 6.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
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FS
type: SiteQuality
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MQRankSum
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -3.108e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.68e-1

DP
type: SiteQuality
SIO_000300: 1.78398e6

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.03342838075593e-5
allele num: 65932
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.545e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.6e0

FS
type: SiteQuality
SIO_000300: 8.7e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.08e0

MQRankSum
type: SiteQuality
SIO_000300: 1.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.2e0

DP
type: SiteQuality
SIO_000300: 1.809154e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9.695559433779329e-5
allele num: 10314
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66134
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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DP
type: SiteQuality
SIO_000300: 1.817351e6

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: 6.21e-1

VQSLOD
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ReadPosRankSum
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FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 3.132e1

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 66290
num of homozygotes: 0

African
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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ClippingRankSum
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FS
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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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variant carriers: 0

Other
type: Population
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allele num: 900
num of homozygotes: 0

Latino
type: Population
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allele frequency: 8.691117677733357e-5
allele num: 11506
num of homozygotes: 0

South Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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MQRankSum
type: SiteQuality
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BaseQRankSum
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QD
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VQSLOD
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ClippingRankSum
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FS
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ReadPosRankSum
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InbreedingCoeff
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DP
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MQ
type: SiteQuality
SIO_000300: 5.741e1

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

Latino
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allele num: 11520
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
allele num: 900
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European (Non-Finnish)
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allele num: 66452
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African
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South Asian
type: Population
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QD
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BaseQRankSum
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MQRankSum
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DP
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InbreedingCoeff
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VQSLOD
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MQ
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FS
type: SiteQuality
SIO_000300: 2.666e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.639999999999999e-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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bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

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

East Asian
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allele count: 1
allele frequency: 1.160362032954282e-4
allele num: 8618
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66486
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.29e0

DP
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 2.0e-4

QD
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SIO_000300: 1.113e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.106e0

MQRankSum
type: SiteQuality
SIO_000300: 7.1e-1

FS
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SIO_000300: 0.0e0

VQSLOD
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SIO_000300: 2.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.7e-1

MQ
type: SiteQuality
SIO_000300: 5.958e1

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501366243281386e-5
allele num: 66606
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -1.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.97e-1

QD
type: SiteQuality
SIO_000300: 1.366e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.9e-1

DP
type: SiteQuality
SIO_000300: 1.830886e6

VQSLOD
type: SiteQuality
SIO_000300: 9.64e-1

FS
type: SiteQuality
SIO_000300: 3.401e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.47e0

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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variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.21256214380987e-4
allele num: 16494
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66634
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 8.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.248e0

QD
type: SiteQuality
SIO_000300: 1.191e1

MQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.832824e6

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.158748551564311e-4
allele num: 8630
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66638
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 9.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.65e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.179999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.91e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.83e-1

QD
type: SiteQuality
SIO_000300: 1.548e1

DP
type: SiteQuality
SIO_000300: 1.833067e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.502100588164687e-5
allele num: 66648
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.658008658008658e-5
allele num: 11550
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 1.833865e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.48e-1

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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FS
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QD
type: SiteQuality
SIO_000300: 1.232e1

VQSLOD
type: SiteQuality
SIO_000300: 3.96e0

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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variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500060002400096e-5
allele num: 66664
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

FS
type: SiteQuality
SIO_000300: 4.322e0

ReadPosRankSum
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MQRankSum
type: SiteQuality
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QD
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MQ
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DP
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VQSLOD
type: SiteQuality
SIO_000300: 5.15e-1

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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GenotypeQuality
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variant carriers: 0

African
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allele count: 1
allele frequency: 9.633911368015414e-5
allele num: 10380
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8636
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.500180007200288e-5
allele num: 66664
num of homozygotes: 0

Other
type: Population
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MQ
type: SiteQuality
SIO_000300: 5.97e1

MQRankSum
type: SiteQuality
SIO_000300: 5.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
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VQSLOD
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QD
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DP
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FS
type: SiteQuality
SIO_000300: 1.148e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.112e0

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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variant carriers: 0

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

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

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

South Asian
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allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

East Asian
type: Population
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allele frequency: 0.0e0
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African
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.734e0

FS
type: SiteQuality
SIO_000300: 1.56e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.46e-1

QD
type: SiteQuality
SIO_000300: 8.56e0

VQSLOD
type: SiteQuality
SIO_000300: 7.4e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.835078e6

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

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

GenotypeQuality
all individuals: 130
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2857
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 7081
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7290
bin: 9.75e1
variant carriers: 54

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

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2161
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2196
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36050
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1416
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 888
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 2.596503375454388e-4
allele num: 11554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.5036768016328e-5
allele num: 66634
num of homozygotes: 0

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

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

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

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

South Asian
type: Population
allele count: 49
allele frequency: 2.971497877501516e-3
allele num: 16490
num of homozygotes: 3

FS
type: SiteQuality
SIO_000300: 1.151e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.67e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.77e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.44e-1

QD
type: SiteQuality
SIO_000300: 1.298e1

DP
type: SiteQuality
SIO_000300: 1.836635e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.921e0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1416
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 95
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 888
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2196
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2857
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2161
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7290
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 191
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7081
bin: 6.75e1
variant carriers: 0

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.00147072065312e-5
allele num: 66634
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-2

FS
type: SiteQuality
SIO_000300: 1.151e0

MQRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.77e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.921e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

DP
type: SiteQuality
SIO_000300: 1.836635e6

QD
type: SiteQuality
SIO_000300: 1.298e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.67e-1

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 69
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 885
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2839
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2156
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1419
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 132
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7056
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35881
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7242
bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502042778178322e-5
allele num: 66576
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.87e-1

FS
type: SiteQuality
SIO_000300: 9.93e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.51e-1

DP
type: SiteQuality
SIO_000300: 1.832994e6

MQ
type: SiteQuality
SIO_000300: 5.919e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.100000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.107e1

GenotypeQuality
all individuals: 1419
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 885
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2838
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7046
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2153
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 341
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35911
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2185
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7242
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 76
bin: 3.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.024803387779795e-4
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

QD
type: SiteQuality
SIO_000300: 1.302e1

DP
type: SiteQuality
SIO_000300: 1.83336e6

FS
type: SiteQuality
SIO_000300: 9.045e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.441e0

VQSLOD
type: SiteQuality
SIO_000300: 4.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-2

GenotypeQuality
all individuals: 93
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2154
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 506
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variant carriers: 0

GenotypeQuality
all individuals: 7016
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 215
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35558
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 886
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2829
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2180
bin: 7.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.158748551564311e-4
allele num: 8630
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66566
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.259e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.36e0

VQSLOD
type: SiteQuality
SIO_000300: -1.737e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.66e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.68e0

DP
type: SiteQuality
SIO_000300: 1.829099e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

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

GenotypeQuality
all individuals: 2173
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 527
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variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 145
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variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6997
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2151
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2821
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 885
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7241
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 35490
bin: 6.25e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502584445245823e-5
allele num: 66552
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.828668e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.422e0

MQRankSum
type: SiteQuality
SIO_000300: 1.17e-1

FS
type: SiteQuality
SIO_000300: 1.749e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.45e-1

QD
type: SiteQuality
SIO_000300: 6.23e0

VQSLOD
type: SiteQuality
SIO_000300: 3.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.3e-2

GenotypeQuality
all individuals: 35457
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7005
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2173
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 565
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variant carriers: 0

GenotypeQuality
all individuals: 7242
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 110
bin: 5.75e1
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GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1419
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2832
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2153
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502494140272853e-5
allele num: 66556
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.82758e6

QD
type: SiteQuality
SIO_000300: 1.589e1

FS
type: SiteQuality
SIO_000300: 1.105e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.56e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.94e0

GenotypeQuality
all individuals: 110
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2165
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6965
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1418
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2823
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35182
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 176
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7241
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2150
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 885
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66528
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.073120369245719e-5
allele num: 16466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.120000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.109e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.02e-1

QD
type: SiteQuality
SIO_000300: 1.933e1

DP
type: SiteQuality
SIO_000300: 1.825568e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2144
bin: 7.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
all individuals: 8
bin: 1.25e1
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GenotypeQuality
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bin: 6.25e1
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: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7238
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 882
bin: 8.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504483360414034e-5
allele num: 66468
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.805263e6

QD
type: SiteQuality
SIO_000300: 1.158e1

FS
type: SiteQuality
SIO_000300: 4.372e0

MQRankSum
type: SiteQuality
SIO_000300: 6.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 882
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 196
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66468
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.671179883945841e-5
allele num: 10340
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

QD
type: SiteQuality
SIO_000300: 1.158e1

MQRankSum
type: SiteQuality
SIO_000300: 6.41e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 9.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

FS
type: SiteQuality
SIO_000300: 4.372e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

DP
type: SiteQuality
SIO_000300: 1.805263e6

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6703
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7236
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1417
bin: 9.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504166541319455e-5
allele num: 66482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.032e0

FS
type: SiteQuality
SIO_000300: 1.935e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.75e0

VQSLOD
type: SiteQuality
SIO_000300: 5.93e-1

QD
type: SiteQuality
SIO_000300: 1.187e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.547e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

DP
type: SiteQuality
SIO_000300: 1.799812e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

GenotypeQuality
all individuals: 875
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 310
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6625
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 880
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variant carriers: 0

GenotypeQuality
all individuals: 295
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variant carriers: 0

GenotypeQuality
all individuals: 1396
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66470
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159823706796567e-4
allele num: 8622
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

DP
type: SiteQuality
SIO_000300: 1.793183e6

VQSLOD
type: SiteQuality
SIO_000300: 5.05e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.64e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.3e-2

QD
type: SiteQuality
SIO_000300: 1.391e1

MQ
type: SiteQuality
SIO_000300: 5.972e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.48e0

GenotypeQuality
all individuals: 1075
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 874
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variant carriers: 1

GenotypeQuality
all individuals: 525
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 28
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 1625
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GenotypeQuality
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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: 90

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2736
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 85
allele frequency: 8.231648266511718e-3
allele num: 10326
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

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

Latino
type: Population
allele count: 5
allele frequency: 4.336513443191674e-4
allele num: 11530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66420
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

FS
type: SiteQuality
SIO_000300: 8.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.783089e6

MQRankSum
type: SiteQuality
SIO_000300: 2.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.57e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.44e0

QD
type: SiteQuality
SIO_000300: 1.52e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2600
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16336
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10096
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.732099196646873e-5
allele num: 11452
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65614
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.791523e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

QD
type: SiteQuality
SIO_000300: 1.144e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 7.43e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-2

GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9824
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8896
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6886
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.435176462062468e-5
allele num: 55196
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6002
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14418
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.61e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.01e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.02e-1

DP
type: SiteQuality
SIO_000300: 1.157881e6

QD
type: SiteQuality
SIO_000300: 1.345e1

GenotypeQuality
all individuals: 499
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 841
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6886
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9824
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6002
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55196
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.935774726036899e-5
allele num: 14418
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8896
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.43e-1

QD
type: SiteQuality
SIO_000300: 1.345e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.61e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.09e-1

DP
type: SiteQuality
SIO_000300: 1.157881e6

GenotypeQuality
all individuals: 104
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1449
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.735749496632646e-5
allele num: 57612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7400
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9172
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14694
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10276
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6120
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.270107e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.51e-1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.562e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.266e0

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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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6142
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.453396415374521e-5
allele num: 57914
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.035002035002035e-4
allele num: 14742
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9196
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7458
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.216e1

FS
type: SiteQuality
SIO_000300: 5.607e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.77e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.280017e6

MQRankSum
type: SiteQuality
SIO_000300: 4.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

GenotypeQuality
all individuals: 44
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variant carriers: 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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bin: 9.75e1
variant carriers: 1398

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8292
num of homozygotes: 0

Latino
type: Population
allele count: 115
allele frequency: 1.041477993117189e-2
allele num: 11042
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 48
allele frequency: 7.521153243497336e-3
allele num: 6382
num of homozygotes: 0

South Asian
type: Population
allele count: 19
allele frequency: 1.22060901965823e-3
allele num: 15566
num of homozygotes: 0

African
type: Population
allele count: 37
allele frequency: 3.793315562846012e-3
allele num: 9754
num of homozygotes: 0

Other
type: Population
allele count: 13
allele frequency: 1.494252873563218e-2
allele num: 870
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1186
allele frequency: 1.887332908975175e-2
allele num: 62840
num of homozygotes: 8

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.88e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.285e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.469e0

MQRankSum
type: SiteQuality
SIO_000300: 1.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

DP
type: SiteQuality
SIO_000300: 1.428922e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.1e0

GenotypeQuality
all individuals: 800
bin: 7.25e1
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: 191
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9822
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6410
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.382435537401073e-5
allele num: 15668
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11118
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.579629103086595e-5
allele num: 63306
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8350
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.56e-1

DP
type: SiteQuality
SIO_000300: 1.419045e6

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.49e0

MQRankSum
type: SiteQuality
SIO_000300: 9.3e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

QD
type: SiteQuality
SIO_000300: 1.151e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.68e-1

FS
type: SiteQuality
SIO_000300: 2.08e0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10006
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11294
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.108196313679172e-5
allele num: 64346
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15966
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6480
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -6.764e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 8.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.65e-1

DP
type: SiteQuality
SIO_000300: 1.441539e6

FS
type: SiteQuality
SIO_000300: 2.081e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.35e-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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bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16032
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11314
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64590
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10058
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6494
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.17343346632246e-4
allele num: 8522
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.093e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.49e-1

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.447306e6

VQSLOD
type: SiteQuality
SIO_000300: -2.212e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.809020436927414e-5
allele num: 11352
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6524
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65184
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.458476e6

InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 6.909999999999999e-1

FS
type: SiteQuality
SIO_000300: 1.84e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.38e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

QD
type: SiteQuality
SIO_000300: 1.48e1

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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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.51846452866861e-5
allele num: 65856
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
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FS
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QD
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.473727e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

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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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66108
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African
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allele frequency: 0.0e0
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South Asian
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allele count: 1
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allele num: 16396
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Latino
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Other
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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QD
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DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.92e1

FS
type: SiteQuality
SIO_000300: 1.462e0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10290
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South Asian
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allele num: 16400
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Other
type: Population
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allele frequency: 0.0e0
allele num: 900
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Latino
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6582
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8618
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66148
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
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FS
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MQRankSum
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -2.04e-1

DP
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SIO_000300: 1.481244e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.12e-1

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10312
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Latino
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allele count: 16
allele frequency: 1.392757660167131e-3
allele num: 11488
num of homozygotes: 0

European (Non-Finnish)
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allele count: 36
allele frequency: 5.433306166802499e-4
allele num: 66258
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.111111111111111e-3
allele num: 900
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16410
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.12e-1

DP
type: SiteQuality
SIO_000300: 1.484294e6

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.386e1

VQSLOD
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SIO_000300: 5.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.67e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.962e1

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16414
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 8.70170553428472e-5
allele num: 11492
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African
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East Asian
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DP
type: SiteQuality
SIO_000300: 1.483377e6

FS
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VQSLOD
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MQRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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QD
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BaseQRankSum
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ReadPosRankSum
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